company
Philips North America Llc
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-07-01Philips North America Llc — Class II recall: Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the follo…
- fda_recall · device_recall2026-07-01Philips North America Llc — Class II recall: Philips Avalon Fetal Monitor, FM 30 Part numberM2703A
- fda_recall · device_recall2026-07-01Philips North America Llc — Class II recall: Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A
- fda_recall · device_recall2026-06-17Philips North America Llc — Class II recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Frequently asked questions
- How many FDA warning letters has Philips North America Llc received?
- Argus HQ has not recorded an FDA warning letter for Philips North America Llc in our current dataset.
- What FDA recalls has Philips North America Llc issued?
- Argus HQ has recorded 4 FDA recalls tied to Philips North America Llc.
- Is Philips North America Llc FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 4 recalls, and 0 approval records for Philips North America Llc. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.