FDA Class II Recall: IntelliVue Patient Monitor MX550 with L.x and M.x;… by Philips North America Llc — Recall Details

Key facts

What this classification means

A Class II recall is FDA’s middle classification. FDA assigns Class II when use of, or exposure to, the recalled product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. FDA still requires the recalling firm to notify affected accounts and submit status reports on the correction, though the monitoring intensity is lower than for a Class I recall. FDA's Center for Devices and Radiological Health (for devices) or Center for Drug Evaluation and Research (for drugs) reviews the classification and can require additional corrective action if the initial response is judged insufficient. Because this record is filed as Class II, professionals and consumers handling an affected lot should treat FDA's own classification -- not this page's summary of it -- as the authoritative risk signal. A Class I recall is FDA’s most serious classification. FDA assigns Class I when there is a reasonable probability that use of, or exposure to, the recalled product will cause serious adverse health consequences or death. This classification does not mean harm has already occurred in every case -- it reflects FDA’s assessment of the realistic worst-case risk profile of the defect described in the recall, based on the reason for recall reported by the firm. Class I recalls receive the closest FDA monitoring of the three classes: the recalling firm typically must submit a recall strategy, periodic status reports, and effectiveness checks confirming that the affected lots have actually been removed from distribution or corrected in the field.

What consumers should do

Facilities, clinicians, and consumers holding an affected unit or lot of IntelliVue Patient Monitor MX550 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866066. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates. should stop using it for the purpose described in the recall notice and hold remaining stock pending instructions from Philips North America Llc. FDA recall records typically direct the recalling firm to notify known accounts directly with a recall letter describing the specific corrective action -- replacement, field correction, refund, or return. Anyone who received the product through a distributor rather than directly from Philips North America Llc should confirm with their supplier whether their specific lot or unit is on the affected list, since recall notices are lot- or unit-specific and not every unit of a product line is necessarily included. Questions about a specific unit's status should go to Philips North America Llc directly or to the distributor that supplied it; Argus HQ is a public-record aggregator, not the recalling firm, and cannot confirm individual unit status.

Philips North America’s FDA history

Argus HQ has recorded 355 total FDA actions tied to Philips North America: 0 warning letters, 355 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

What is the FDA recall number for this event?

FDA recall number Z-2511-2024.

What is the current status of this recall?

Status as recorded by FDA: Ongoing.

Where can I verify this recall directly with FDA?

The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.

Is IntelliVue Patient Monitor MX550 with L.x and M.x; K.x provi recalled?

Yes. FDA lists a Class II recall by Philips North America Llc for IntelliVue Patient Monitor MX550 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866066. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates., reported 20240814, with status "Ongoing." FDA recall number: Z-2511-2024.

Related enforcement actions

• Recall: Philips North America Llc — Class II recall: Spectral CT; Product Code (REF): 728333; →
• Recall: Philips North America Llc — Class II recall: Spectral CT 7500 on Rails; Product Code (REF): 728334; →
• Recall: Philips North America Llc — Class II recall: IQon Spectral CT; Product Code (REF): 728332; →
• Recall: Philips North America Llc — Class II recall: Brilliance iCT; Product Code (REF): 728306; →
• Recall: Philips North America — Class II recall: Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW… →
• Recall: Philips North America — Class II recall: SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with S… →
• Recall: Philips North America — Class II recall: Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. M… →
• Recall: Philips North America — Class II recall: Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR syst… →