FDA enforcement deep dive

Philips North America: FDA Enforcement History

Name: FDA Enforcement Actions Against Philips North America
Creator: Argus HQ
License: https://argushq.ai/methodology

Most recent tracked FDA action: July 1, 2026

Philips North America carries the largest tracked FDA device-recall record in the Argus HQ database: 355 recalls, dominated by the multi-year Respironics sleep-and-respiratory-device field action alongside a steady stream of smaller device corrections. The pattern below is computed directly from Argus HQ’s FDA-sourced event records -- recall velocity, severity mix, and recurring reason categories -- not editorial commentary.

FDA action counts (Argus HQ database)

Total tracked FDA actions	355
Recalls	355
Warning letters	0
Form 483 inspection citations	0
Most recent tracked action	July 1, 2026
Most severe rating on file	critical

Recall severity breakdown

Computed from all 355 tracked recalls. FDA classifies each recall Class I (most serious), II, or III on the underlying record; Argus HQ maps that to critical/high/medium/low severity buckets.

high	342 (96.3%)
critical	7 (2.0%)
medium	6 (1.7%)

Recall velocity by month

Months with at least one tracked recall for Philips North America, oldest to most recent. Gaps indicate months with zero tracked recalls, not missing data.

Month	Recalls
2023-01	1
2023-04	4
2023-05	7
2023-06	2
2023-07	1
2023-08	10
2023-09	1
2023-10	2
2023-11	28
2023-12	2
2024-01	14
2024-02	20
2024-04	44
2024-05	37
2024-06	3
2024-07	4
2024-08	4
2024-10	18
2024-12	15
2025-02	5
2025-04	6
2025-05	19
2025-06	9
2025-07	1
2025-08	19
2025-10	12
2025-12	25
2026-01	2
2026-02	17
2026-05	19
2026-06	1
2026-07	3

Recurring recall-reason patterns

Argus HQ keyword-matched the free-text “reason for recall” field on each tracked record into categories below. FDA does not publish a structured reason code for device recalls, so this is Argus HQ’s own pattern analysis, not an official FDA classification — records that don’t match a listed keyword fall into “Other.”

Other / not pattern-matched	321 recalls
Software	18 recalls
Labeling	16 recalls

Full recall history (355)

Most recent first. Every row links to its Argus HQ record and FDA.gov source.

Date	Severity	Title
2026-07-01	high	Philips North America Llc — Class II recall: Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the follo…
2026-07-01	high	Philips North America Llc — Class II recall: Philips Avalon Fetal Monitor, FM 30 Part numberM2703A
2026-07-01	high	Philips North America Llc — Class II recall: Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A
2026-06-17	high	Philips North America Llc — Class II recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
2026-05-06	high	Philips North America — Class II recall: Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (…
2026-05-06	high	Philips North America — Class II recall: Philips Evolution upgrade 3.0T with MR Elastography (MRE). 1. Model Number (…
2026-05-06	high	Philips North America — Class II recall: Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model N…
2026-05-06	high	Philips North America — Class II recall: Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF)…
2026-05-06	high	Philips North America — Class II recall: Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model N…
2026-05-06	high	Philips North America — Class II recall: Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model…
2026-05-06	high	Philips North America — Class II recall: Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF)…
2026-05-06	high	Philips North America — Class II recall: Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 7812…
2026-05-06	high	Philips North America — Class II recall: Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1.…
2026-05-06	high	Philips North America — Class II recall: Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF)…
2026-05-06	high	Philips North America — Class II recall: Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 7813…
2026-05-06	high	Philips North America — Class II recall: Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 7811…
2026-05-06	high	Philips North America — Class II recall: Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 7813…
2026-05-06	high	Philips North America — Class II recall: Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Num…
2026-05-06	high	Philips North America — Class II recall: Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120.…
2026-05-06	high	Philips North America — Class II recall: Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF):…
2026-05-06	high	Philips North America — Class II recall: Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 7…
2026-05-06	high	Philips North America — Class II recall: Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 7…
2026-05-06	high	Philips North America — Class II recall: Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF):…
2026-02-18	high	Philips North America Llc — Class II recall: Spectral CT; Product Code (REF): 728333;
2026-02-18	high	Philips North America Llc — Class II recall: Spectral CT 7500 on Rails; Product Code (REF): 728334;
2026-02-18	high	Philips North America Llc — Class II recall: IQon Spectral CT; Product Code (REF): 728332;
2026-02-18	high	Philips North America Llc — Class II recall: Brilliance iCT; Product Code (REF): 728306;
2026-02-04	high	Philips North America — Class II recall: Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW…
2026-02-04	high	Philips North America — Class II recall: SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with S…
2026-02-04	high	Philips North America — Class II recall: Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. M…
2026-02-04	high	Philips North America — Class II recall: Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR syst…
2026-02-04	high	Philips North America — Class II recall: MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems with SW vers…
2026-02-04	high	Philips North America — Class II recall: Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with SW versi…
2026-02-04	high	Philips North America — Class II recall: Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377. MR systems with SW…
2026-02-04	high	Philips North America — Class II recall: Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137. MR…
2026-02-04	high	Philips North America — Class II recall: Ingenia Ambition S. Product Code (REF): 782108. MR systems with SW version R…
2026-02-04	high	Philips North America — Class II recall: Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.…
2026-02-04	high	Philips North America — Class II recall: Ingenia Ambition X. Product Code (REF): (1) 781356, (2) 782109, (3)782138. M…
2026-02-04	high	Philips North America — Class II recall: SmartPath to dStream for XR and 3.0T. Product Code (REF): 781270. MR systems…
2026-02-04	high	Philips North America — Class II recall: Upgrade to MR 7700. Product Code (REF): 782130. MR systems with SW version R…
2026-01-28	high	Philips North America — Class II recall: Patient Information Center iX; Software Version Number: 4.5.0
2026-01-14	high	Philips North America Llc — Class II recall: Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.
2025-12-17	high	Philips North America — Class II recall: Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTI…
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP90. Product Number: M8010A.
2025-12-10	high	Philips North America Llc — Class II recall: Incisive CT; Software Version Number: 4.5, 5.0, 5.1;
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX400. Product Number: 866060.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP20. Product Number: M8001A.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP5. Product Number: M8105A.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX750. Product Number: 866471.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP80. Product Number: M8008A.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX800. Product Number: 865240.
2025-12-10	high	Philips North America Llc — Class II recall: CT 5300; Software Version Number: 4.5, 5.0, 5.1;
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP60. Product Number: M8005A.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX450. Product Number: 866062.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX850. Product Number: 866470.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP30. Product Number: M8002A.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP70. Product Number: M8007A.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP2. Product Number: M8102A.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX100. Product Number: 867033.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Multi-Measurement Module X3. Product Number: 867030.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX600. Product Number: 865242.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP50. Product Number: M8004A.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue MP40. Product Number: M8003A.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX550. Product Number: 866066.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX500. Product Number: 866064.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX700. Product Number: 865241.
2025-12-10	high	Philips North America Llc — Class II recall: IntelliVue Multi Measurement Server X2. Product Number: M3002A.
2025-10-22	high	Philips North America — Class II recall: Cardiac Workstation 7000; Model Number: 860441;
2025-10-22	high	Philips North America — Class II recall: Cardiac Workstation 5000; Model Number: 860439;
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. Brilliance iCT SP, Model Numb…
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 72…
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Nu…
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Mod…
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. Ingenuity Core128 / Elite Chi…
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307…
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, M…
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number:…
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. IQon Spectral CT, Model Numbe…
2025-10-01	high	Philips North America Llc — Class II recall: Philips CT systems labeled as the following: 1. Brilliance 16 Power, Model Nu…
2025-08-06	high	Philips North America — Class II recall: Evolution Upgrade 1.5T Model Numbers (REF): (1) 782116, (2) 782148;
2025-08-06	high	Philips North America — Class II recall: Upgrade to MR 7700 Model Number (REF): 782130;
2025-08-06	high	Philips North America — Class II recall: Ingenia Ambition S Model Numbers (REF): (1) 781359, (2) 782108, (3) 782133 (Chi…
2025-08-06	high	Philips North America — Class II recall: Ingenia 3.0T Model Numbers (REF): (1) 781342, (2) 781377, (3) 782103;
2025-08-06	high	Philips North America — Class II recall: Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117, (2) 782143;
2025-08-06	high	Philips North America — Class II recall: Ingenia Elition S Model Numbers (REF): (1) 781357, (2) 782106, (3) 782137, (4)…
2025-08-06	high	Philips North America — Class II recall: Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105;
2025-08-06	high	Philips North America — Class II recall: Ingenia 1.5T S Model Number (REF): 781347;
2025-08-06	high	Philips North America — Class II recall: Achieva 3.0T; Model Numbers (REF): (1) 781177, (2) 781277, (3) 781278, (4) 781…
2025-08-06	high	Philips North America — Class II recall: MR 5300 Model Numbers (REF): (1) 782110, (2) 782135 (China ONLY), (3) 782152;
2025-08-06	high	Philips North America — Class II recall: SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 78211…
2025-08-06	high	Philips North America — Class II recall: Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138;
2025-08-06	high	Philips North America — Class II recall: SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118, (2) 782144;
2025-08-06	high	Philips North America — Class II recall: MR 7700 Model Numbers (REF): (1) 782120, (2) 782153;
2025-08-06	high	Philips North America — Class II recall: SmartPath to dStream for 3.0T Model Number (REF): 782145;
2025-08-06	high	Philips North America — Class II recall: Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 78210…
2025-08-06	high	Philips North America — Class II recall: Achieva XR; Model Numbers (REF): (1) 781153, (2) 781253;
2025-08-06	high	Philips North America — Class II recall: Intera 3.0T Quasar Dual Model Number (REF): 781150;
2025-08-06	high	Philips North America — Class II recall: Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4)…
2025-07-02	high	Philips North America Llc — Class II recall: Spectral CT. Computed tomography X-ray system.
2025-06-18	high	Philips North America — Class II recall: Intera 1.5T Omni/Stellar; Product Number: 781104;
2025-06-18	high	Philips North America — Class II recall: Intera 1.5T Achieva Nova-Dual Product Number: 781173;
2025-06-18	high	Philips North America — Class II recall: Intera 1.5T Explorer/Nova Dual Product Number: 781108;
2025-06-18	high	Philips North America — Class II recall: Intera 1.5T Achieva Nova Product Number: 781172;
2025-06-18	high	Philips North America — Class II recall: Achieva XR Product Numbers: (1) 781153, (2) 781253;
2025-06-18	high	Philips North America — Class II recall: SmartPath to dStream for 1.5T¿; Product Number: 782146;
2025-06-18	high	Philips North America — Class II recall: Intera 1.5T Achieva IT Nova Product Number: 781175
2025-06-18	high	Philips North America — Class II recall: Intera 1.5T Master/Nova Product Number: 781106;
2025-06-18	high	Philips North America — Class II recall: Intera Achieva 1.5T Pulsar; Product Number: 781171;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 78…
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 78…
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782…
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Ingenia 3.0T CX; Model Number: 781271;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782…
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 78…
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: SmartPath to dStream for 3.0T; Model Number: 782145
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Upgrade to MR 7700; Model Number: 782130;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Ingenia 1.5T S; Model Number: 781347;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: SmartPath to dStream for XR and 3.0T; Model Numbers: (1) 781270,…
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782…
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Ingenia 1.5T CX; Model Number: 781262;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
2025-05-28	high	Philips North America Llc — Class II recall: Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396,…
2025-05-14	high	Philips North America Llc — Class II recall: Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pe…
2025-04-30	high	Philips North America Llc — Class II recall: Zenition 50. Product Code 718096. The devices are used for radiological guidanc…
2025-04-30	high	Philips North America Llc — Class II recall: Zenition 70. Product Code 718133. The devices are used for radiological guidance…
2025-04-30	high	Philips North America Llc — Class II recall: Veradius Unity. Product Code 718132. The devices are used for radiological guida…
2025-04-30	high	Philips North America Llc — Class II recall: Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomograph…
2025-04-23	high	Philips North America Llc — Class II recall: Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.
2025-04-23	high	Philips North America Llc — Class II recall: Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
2025-02-12	high	Philips North America Llc — Class II recall: IntelliBridge EC10 Module. Model Number: 865115
2025-02-12	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX450. Model Number: 866062
2025-02-12	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX550. Model Number: 866066
2025-02-12	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX500. Model Number: 866064
2025-02-12	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX400. Model Number: 866060
2024-12-25	high	Philips North America Llc — Class II recall: Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216
2024-12-11	high	Philips North America Llc — Class II recall: Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.
2024-12-04	high	Philips North America Llc — Class II recall: Mammotrak Interventional Coil 1.5T
2024-12-04	high	Philips North America Llc — Class II recall: Mammotrak Diagnostic Coil 1.5T
2024-12-04	high	Philips North America Llc — Class II recall: Mammotrak Interventional Coil 3.0T
2024-12-04	high	Philips North America Llc — Class II recall: dS Breast 16ch 3.0T
2024-12-04	high	Philips North America Llc — Class II recall: dS Breast 16ch 1.5T
2024-12-04	high	Philips North America Llc — Class II recall: ST SENSE Breast Coil
2024-12-04	high	Philips North America Llc — Class II recall: Achieva TX Interventional Coil 3.0T
2024-12-04	high	Philips North America Llc — Class II recall: ST SENSE Breast Dx Coil
2024-12-04	high	Philips North America Llc — Class II recall: dS Breast 7ch 1.5T
2024-12-04	high	Philips North America Llc — Class II recall: SENSE Breast Coil
2024-12-04	high	Philips North America Llc — Class II recall: Mammotrak Diagnostic Coil 3.0T
2024-12-04	high	Philips North America Llc — Class II recall: dS Breast 7ch 3.0T
2024-12-04	high	Philips North America Llc — Class II recall: SENSE Breast Coil 3.0T 7ch
2024-10-16	high	Philips North America — Class II recall: Patient Information Center iX, Product Code 866386, and Patient Information Cent…
2024-10-16	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01…
2024-10-09	high	Philips North America — Class II recall: IntelliVue G7m Anesthesia Gas Module, Product Number 866173
2024-10-09	high	Philips North America Llc — Class II recall: DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system…
2024-10-02	high	Philips North America Llc — Class II recall: Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional image…
2024-10-02	high	Philips North America Llc — Class II recall: Ingenia Ambition S - For use as a diagnostic device to obtain cross-sectional im…
2024-10-02	high	Philips North America Llc — Class II recall: SmartPath to dStream for 1.5T - For use as a diagnostic device to obtain cross-s…
2024-10-02	high	Philips North America Llc — Class II recall: Ingenia Elition X- For use as a diagnostic device to obtain cross-sectional imag…
2024-10-02	high	Philips North America Llc — Class II recall: Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, s…
2024-10-02	high	Philips North America Llc — Class II recall: Ingenia Ambition X - For use as a diagnostic device to obtain cross-sectional im…
2024-10-02	high	Philips North America Llc — Class II recall: MR 5300 - For use as a diagnostic device to obtain cross-sectional images, spect…
2024-10-02	high	Philips North America — Class II recall: IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 8660…
2024-10-02	high	Philips North America Llc — Class II recall: Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional images,…
2024-10-02	high	Philips North America Llc — Class II recall: Ingenia Elition S -For use as a diagnostic device to obtain cross-sectional imag…
2024-10-02	high	Philips North America Llc — Class II recall: Evolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectiona…
2024-10-02	high	Philips North America Llc — Class II recall: MR 7700 -For use as a diagnostic device to obtain cross-sectional images, spect…
2024-10-02	high	Philips North America Llc — Class II recall: SmartPath to dStream for XR and 3.0T- For use as a diagnostic device to obtain…
2024-10-02	high	Philips North America Llc — Class II recall: SmartPath to Ingenia Elition X - For use as a diagnostic device to obtain cross-…
2024-08-14	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX500 with L.x and M.x; K.x provided with L.x entitle…
2024-08-14	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX550 with L.x and M.x; K.x provided with L.x entitle…
2024-08-14	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX450 with L.x and M.x; K.x provided with L.x entitl…
2024-08-14	high	Philips North America Llc — Class II recall: IntelliVue Patient Monitor MX400 with L.x and M.x; K.x provided with L.x entitle…
2024-07-10	high	Philips North America Llc — Class II recall: Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the feta…
2024-07-03	critical	Philips North America Llc — Class I recall: SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil for torso and abdomen…
2024-07-03	critical	Philips North America Llc — Class I recall: SENSE XL TORSO COIL 3.0T. 16-element receive only coil for torso and abdomen ima…
2024-07-03	critical	Philips North America Llc — Class I recall: SENSE XL TORSO COIL 1.5T. 16-element receive only coil for torso and abdomen ima…
2024-06-12	high	Philips North America Llc — Class II recall: HA FlexTrak II-Patient transport functionality to transport the patient from the…
2024-06-12	high	Philips North America Llc — Class II recall: HA FlexTrak-Patient transport functionality to transport the patient from the pr…
2024-06-12	high	Philips North America Llc — Class II recall: HA FlexTrak-Patient transport functionality to transport the patient from the pr…
2024-05-29	high	Philips North America Llc — Class II recall: Ingenia Elition X- Magnetic Resonance (MR) systems are Medical Electrical Syste…
2024-05-29	high	Philips North America Llc — Class II recall: SmartPath to dStream for XR and 3.0T- Magnetic Resonance (MR) systems are Medica…
2024-05-29	high	Philips North America Llc — Class II recall: Ingenia Ambition X- Magnetic Resonance (MR) systems are Medical Electrical Syste…
2024-05-29	high	Philips North America Llc — Class II recall: Achieva 1.5T Conversion- Magnetic Resonance (MR) systems are Medical Electrical…
2024-05-29	high	Philips North America Llc — Class II recall: Achieva 1.5T Initial system Model Number (REF): 781178
2024-05-29	high	Philips North America Llc — Class II recall: Intera 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indi…
2024-05-29	high	Philips North America Llc — Class II recall: Ingenia 1.5T Model Number (REF): (1) 782140; (2) 782115; (3) 782101; (4) 7…
2024-05-29	high	Philips North America Llc — Class II recall: MR RT - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated…
2024-05-29	high	Philips North America Llc — Class II recall: MR RT Upgrades- Magnetic Resonance (MR) systems are Medical Electrical Systems i…
2024-05-29	high	Philips North America Llc — Class II recall: SmartPath to dStream for 3.0T Model Number (REF): 782145
2024-05-29	high	Philips North America Llc — Class II recall: Ingenia Ambition S Model Number (REF): (1) 782139; (2) 782133; (3) 782108;…
2024-05-29	high	Philips North America Llc — Class II recall: Achieva 3.0T for PET -Magnetic Resonance (MR) systems are Medical Electrical Sys…
2024-05-29	high	Philips North America Llc — Class II recall: Ingenia 3.0T CX Model Number (REF): (1) 782105 (2) 781271
2024-05-29	high	Philips North America Llc — Class II recall: MR 5300- Magnetic Resonance (MR) systems are Medical Electrical Systems indicat…
2024-05-29	high	Philips North America Llc — Class II recall: Evolution upgrade 1.5T- Magnetic Resonance (MR) systems are Medical Electrical…
2024-05-29	high	Philips North America Llc — Class II recall: AchievaXR -Magnetic Resonance (MR) systems are Medical Electrical Systems indica…
2024-05-29	high	Philips North America Llc — Class II recall: Achieva 3.0T TX for PET Model Number (REF): 781479
2024-05-29	high	Philips North America Llc — Class II recall: MR system 1.5T Marlin- Magnetic Resonance (MR) systems are Medical Electrical S…
2024-05-29	high	Philips North America Llc — Class II recall: Sonalleve MR HIFU 3.0T - Magnetic Resonance (MR) systems are Medical Electrical…
2024-05-29	high	Philips North America Llc — Class II recall: Incisive CT - Computed Tomography X-Ray System intended to produce cross-section…
2024-05-29	high	Philips North America Llc — Class II recall: Achieva 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems ind…
2024-05-29	high	Philips North America Llc — Class II recall: Marlin 1.5T - Magnetic Resonance (MR) systems are Medical Electrical Systems ind…
2024-05-29	high	Philips North America Llc — Class II recall: Incisive CT - Computed Tomography X-Ray System intended to produce cross-section…
2024-05-29	high	Philips North America Llc — Class II recall: SmartPath to dStream for 1.5T- Magnetic Resonance (MR) systems are Medical Elect…
2024-05-29	high	Philips North America Llc — Class II recall: Panorama HFO- Magnetic Resonance (MR) systems are Medical Electrical Systems ind…
2024-05-29	high	Philips North America Llc — Class II recall: Achieva 3.0T Model Number (REF): (1) 781345; (2) 781344; (3) 781278; (4)…
2024-05-29	high	Philips North America Llc — Class II recall: Upgrade dStream - Magnetic Resonance (MR) systems are Medical Electrical Systems…
2024-05-29	high	Philips North America Llc — Class II recall: Ingenia 1.5T S Model Number (REF): 781347
2024-05-29	high	Philips North America Llc — Class II recall: SmartPath to Ingenia Elition X - Magnetic Resonance (MR) systems are Medical Ele…
2024-05-29	high	Philips North America Llc — Class II recall: Evolution upgrade 3.0T Model Number (REF): (1)782117; (2) 782143
2024-05-29	high	Philips North America Llc — Class II recall: Ingenia 1.5T CX - Magnetic Resonance (MR) systems are Medical Electrical System…
2024-05-29	high	Philips North America Llc — Class II recall: Ingenia 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems ind…
2024-05-22	high	Philips North America Llc — Class II recall: Ingenia 1.5T with Evolution Upgrade 1.5T - Magnetic Resonance (MR) systems are M…
2024-05-22	high	Philips North America Llc — Class II recall: Ingenia 3.0T with Evolution Upgrade 3.0T - - Magnetic Resonance (MR) systems are…
2024-05-22	high	Philips North America Llc — Class II recall: Patient Information Center iX and Patient Information Center iX Expand, Software…
2024-05-08	high	Philips North America Llc — Class II recall: The Oncology Essentials Package of the Spectral CT imaging system.
2024-05-01	high	Philips North America Llc — Class II recall: Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS):…
2024-04-24	high	Philips North America Llc — Class II recall: Achieva 3.0TX for PET, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Ingenia 1.5T, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Ingenia 1.5T CX, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Ingenia Ambition X, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 0.5T Standard, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera CV, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.5T Omni/Stellar, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.0T Power/Pulsar, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Ingenia Ambition S, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: GYROSCAN ACS-NT, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 3.0T Quasar Dual, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.5T Achieva Nova, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.0T Omni/Stellar, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Achieva 3.0T for PET, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.5T Achieva IT Nova, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Achieva 1.5T, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Evolution Upgrade 3.0T, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: MR 7700, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: GYROSCAN T5-NT, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Achieva 3.0T, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.5T, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Ingenia 1.5T S, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Ingenia Elition S, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Ingenia 3.0T, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Enterprise 1.5T, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Achieva 1.5T Initial, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.5T Master/Nova, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: GYROSCAN T5, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Achieva 1.5T Conversion, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.5T R11, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Ingenia 3.0T CX, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: MR 5300, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: GYROSCAN T10-NT, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera Achieva 1.5T Pulsar, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Intera 1.5T Power/Pulsar, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Ingenia Elition X, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: SmartPath to dStream for 1.5T, Magnetic Resonance System.
2024-04-24	high	Philips North America Llc — Class II recall: Achieva XR, Magnetic Resonance System.
2024-04-17	high	Philips North America — Class II recall: PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade…
2024-04-03	high	Philips North America — Class II recall: CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Up…
2024-04-03	high	Philips North America — Class II recall: Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Exp…
2024-02-21	high	Philips North America — Class II recall: ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F)…
2024-02-21	high	Philips North America — Class II recall: ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R…
2024-02-14	critical	Philips North America — Class I recall: BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-di…
2024-02-14	high	Philips North America — Class II recall: Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 98971000…
2024-02-14	critical	Philips North America — Class I recall: BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478;…
2024-02-14	high	Philips North America — Class II recall: Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989…
2024-02-14	high	Philips North America — Class II recall: Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 98…
2024-02-14	critical	Philips North America — Class I recall: BrightView XCT, gamma camera for SPECT; Model Nos.: 6-digit format 882482;…
2024-02-07	high	Philips North America — Class II recall: Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283.
2024-02-07	high	Philips North America — Class II recall: Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261.
2024-02-07	high	Philips North America — Class II recall: SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270, 782113, 782129…
2024-02-07	high	Philips North America — Class II recall: Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105.
2024-02-07	high	Philips North America — Class II recall: Intera Achieva 1.5T Pulsar. Model (REF) Number 781171.
2024-02-07	high	Philips North America — Class II recall: Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.
2024-02-07	high	Philips North America — Class II recall: Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173.
2024-02-07	high	Philips North America — Class II recall: Achieva 1.5T Initial system. Model (REF) Numbers 781178.
2024-02-07	high	Philips North America — Class II recall: Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.
2024-02-07	high	Philips North America — Class II recall: SmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112.
2024-02-07	high	Philips North America — Class II recall: Achieva XR. Model (REF) Numbers 781153, 781253.
2024-02-07	high	Philips North America — Class II recall: Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.
2024-01-31	medium	Philips North America — Class III recall: Intera 1.5T, Model No. 781195
2024-01-31	medium	Philips North America — Class III recall: Achieva 1.5T, Model No. 781178, 781196, 781296
2024-01-31	medium	Philips North America — Class III recall: Ingenia Ambition X, Model No. 782109
2024-01-31	medium	Philips North America — Class III recall: Achieva 3.0T, Model No. 781177
2024-01-31	medium	Philips North America — Class III recall: Achieva 1.5T Conversion, Model No. 781283
2024-01-31	medium	Philips North America — Class III recall: SmartPath to dStream for 1.5T, Model No. 781260, 782112
2024-01-24	high	Philips North America — Class II recall: Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System…
2024-01-24	high	Philips North America Llc — Class II recall: Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.
2024-01-24	high	Philips North America — Class II recall: (1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436
2024-01-24	high	Philips North America — Class II recall: (1) Patient Information Center iX, Model No. 866389 (2) Patient Information Cen…
2024-01-17	high	Philips North America — Class II recall: BrightView X, Gamma Camera, Product Code 882478
2024-01-17	high	Philips North America — Class II recall: (1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product…
2024-01-17	high	Philips North America — Class II recall: BrightView, Gamma Camera System, Product Code 882480.
2024-01-17	high	Philips North America — Class II recall: BrightView XCT, Gamma Camera, Product Code 882482
2023-12-27	high	Philips North America Llc — Class II recall: The device is a whole-body CT x-ray system. The acquired x-ray transmission data…
2023-12-20	critical	Philips North America Llc — Class I recall: Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 7813…
2023-11-29	high	Philips North America Llc — Class II recall: SmartPath to dStream for 1.5T
2023-11-29	high	Philips North America Llc — Class II recall: Achieva 1.5T Conversion
2023-11-29	high	Philips North America Llc — Class II recall: Intera 1.5T Power/Pulsar
2023-11-29	high	Philips North America Llc — Class II recall: Achieva 1.5T
2023-11-29	high	Philips North America Llc — Class II recall: Achieva 1.5T Initial System
2023-11-29	high	Philips North America Llc — Class II recall: Intera 1.5T
2023-11-29	high	Philips North America Llc — Class II recall: Ingenia 1.5T CX
2023-11-22	high	Philips North America Llc — Class II recall: Big Bore RT with software version V4.8.0.10421- Model: 728242 CT scanner and…
2023-11-22	high	Philips North America — Class II recall: Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
2023-11-22	high	Philips North America Llc — Class II recall: Brilliance CT Big Bore Oncology with software version V4.8.0.10421 Model:728243…
2023-11-22	high	Philips North America — Class II recall: Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
2023-11-22	high	Philips North America Llc — Class II recall: Brilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT sc…
2023-11-15	high	Philips North America Llc — Class II recall: DigitalDiagnost 4 Flex/Value, used to acquire, process, store, display and expor…
2023-11-15	high	Philips North America Llc — Class II recall: ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system
2023-11-15	high	Philips North America Llc — Class II recall: DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and…
2023-11-15	high	Philips North America Llc — Class II recall: CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system
2023-11-15	high	Philips North America — Class II recall: BV Endura, BV Pulsera Philips Image Guided Therapy-Systems (IGTS)Mobile Surgery…
2023-11-15	high	Philips North America Llc — Class II recall: DigitalDiagnost C90 High Performance, used to acquire, process, store, display a…
2023-11-15	high	Philips North America Llc — Class II recall: EasyDiagnost Eleva DRF, Release 5, used to acquire, process, store, display and…
2023-11-15	high	Philips North America — Class II recall: Allura Xper IGTS Fixed Systems
2023-11-15	high	Philips North America — Class II recall: Zenition 50 & 70 Mobile Surgery C-arm
2023-11-15	high	Philips North America — Class II recall: Veradius Unity Mobile Surgery C-arm
2023-11-15	high	Philips North America Llc — Class II recall: DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and ex…
2023-11-15	high	Philips North America Llc — Class II recall: DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, displa…
2023-11-15	high	Philips North America Llc — Class II recall: DigitalDiagnost 4 High Performance, used to acquire, process, store, display and…
2023-11-15	high	Philips North America Llc — Class II recall: DigitalDiagnost C90 Release 3, used to acquire, process, store, display and expo…
2023-11-15	high	Philips North America — Class II recall: Integris-Allura IGTS Fixed Systems
2023-11-15	high	Philips North America — Class II recall: Azurion IGTS Fixed Systems
2023-10-11	high	Philips North America Llc — Class II recall: EarlyVue VS30 Vital Signs Monitor, utilizing E01 (Oridion Microstream sidestrea…
2023-10-11	high	Philips North America Llc — Class II recall: EarlyVue VS30 Vitals Monitor, utilizing E01 (Oridion Microstream sidestream etCO…
2023-09-27	high	Philips North America Llc — Class II recall: Patient Information Center iX with Software Version Number 4.x in the following:…
2023-08-16	high	Philips North America — Class II recall: MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgra…
2023-08-16	high	Philips North America — Class II recall: Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107…
2023-08-16	high	Philips North America — Class II recall: MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgra…
2023-08-16	high	Philips North America — Class II recall: Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782…
2023-08-16	high	Philips North America — Class II recall: Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107…
2023-08-16	high	Philips North America — Class II recall: Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782…
2023-08-09	high	Philips North America — Class II recall: Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146
2023-08-09	high	Philips North America — Class II recall: Incisive CT Plus-Computed Tomography X-Ray System Model: 728149
2023-08-09	high	Philips North America — Class II recall: Incisive CT-Computed Tomography X-Ray System Model: 728143
2023-08-09	high	Philips North America — Class II recall: Incisive CT Power (China)-Computed Tomography X-Ray System Model: 728148
2023-07-05	high	Philips North America Llc — Class II recall: DigitalDiagnost C90, Model No. 712034 and 712035
2023-06-07	high	Philips North America Llc — Class II recall: EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01 Product…
2023-06-07	high	Philips North America Llc — Class II recall: EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01 Produ…
2023-05-24	high	Philips North America — Class II recall: CombiDiagnost R90 R1.1
2023-05-24	high	Philips North America — Class II recall: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814
2023-05-24	high	Philips North America — Class II recall: CombiDiagnost R90 R.1.0
2023-05-24	high	Philips North America — Class II recall: ProxiDiagnost N90 R.1.0
2023-05-24	high	Philips North America Llc — Class II recall: Spectral CT 7500 Computed Tomography X-Ray System, Model Number 728333
2023-05-24	high	Philips North America — Class II recall: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813
2023-05-10	high	Philips North America Llc — Class II recall: Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 7…
2023-04-19	high	Philips North America Llc — Class II recall: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers…
2023-04-19	high	Philips North America Llc — Class II recall: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers…
2023-04-19	high	Philips North America Llc — Class II recall: DigitalDiagnost C50 1.1-intended for use in generating radiographic images of hu…
2023-04-19	high	Philips North America Llc — Class II recall: Philips DigitalDiagnost C50 -intended for use in generating radiographic images…
2023-01-18	high	Philips North America Llc — Class II recall: Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate…

Coverage

Respironics field action information for Investor Relations ↗— Philips (company disclosure)
Remediation progress updates ↗— Philips (company disclosure)

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Full FDA history for Philips North America

Other enforcement deep dives

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Verified from FDA.gov · Last updated: Jul 1, 2026

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). Philips North America: FDA Enforcement History. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/enforcement/philips-north-america

MLA

"Philips North America: FDA Enforcement History." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/enforcement/philips-north-america.

Chicago

Argus HQ Research. "Philips North America: FDA Enforcement History." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/enforcement/philips-north-america.

BibTeX

@misc{argushq_argushq_ai_enforcement_philips_north_america_2026,
  title = {Philips North America: FDA Enforcement History},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/enforcement/philips-north-america},
  note = {Accessed: July 23, 2026}
}

Source: FDA.gov (aggregated device recalls) ↗

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