Philips North America Llc: 179 recalls on record

Recalls filed with 1 agency: FDA (179).

First recall on record: April 5, 2017. Most recent: September 9, 2026.

Risk classification: Class I: 5 · Class II: 174

Most recent recalls

DateAgencyProduct
April 24, 2024FDAAchieva XR, Magnetic Resonance System.Z-1556-2024
April 24, 2024FDAAchieva 3.0T, Magnetic Resonance System.Z-1553-2024
April 24, 2024FDAIngenia 3.0T CX, Magnetic Resonance System.Z-1567-2024
April 24, 2024FDAIntera CV, Magnetic Resonance System.Z-1586-2024
April 24, 2024FDAIntera 1.5T Omni/Stellar, Magnetic Resonance System.Z-1581-2024
April 24, 2024FDAIngenia Elition S, Magnetic Resonance System.Z-1570-2024
April 24, 2024FDAIntera 1.5T Master/Nova, Magnetic Resonance System.Z-1580-2024
April 24, 2024FDAIngenia Ambition S, Magnetic Resonance System.Z-1568-2024
April 24, 2024FDASmartPath to dStream for 1.5T, Magnetic Resonance System.Z-1589-2024
April 24, 2024FDAAchieva 3.0TX for PET, Magnetic Resonance System.Z-1555-2024
April 24, 2024FDAMR 7700, Magnetic Resonance System.Z-1588-2024
April 24, 2024FDAIngenia 1.5T, Magnetic Resonance System.Z-1563-2024
April 24, 2024FDAAchieva 1.5T, Magnetic Resonance System.Z-1550-2024
April 24, 2024FDAIntera Achieva 1.5T Pulsar, Magnetic Resonance System.Z-1585-2024
April 24, 2024FDAEvolution Upgrade 3.0T, Magnetic Resonance System.Z-1558-2024
April 24, 2024FDAIntera 1.5T Achieva Nova, Magnetic Resonance System.Z-1577-2024
April 24, 2024FDAAchieva 1.5T Initial, Magnetic Resonance System.Z-1552-2024
April 24, 2024FDAAchieva 1.5T Conversion, Magnetic Resonance System.Z-1551-2024
April 24, 2024FDAIntera 1.5T Power/Pulsar, Magnetic Resonance System.Z-1582-2024
April 24, 2024FDAMR 5300, Magnetic Resonance System.Z-1587-2024
January 24, 2024FDASpectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.Z-0725-2024
December 20, 2023FDAPanorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Phili…Z-0505-2024
November 22, 2023FDABrilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT scanner and…Z-0293-2024
November 15, 2023FDADigitalDiagnost C90 Release 3, used to acquire, process, store, display and export digita…Z-0277-2024
November 15, 2023FDADigitalDiagnost 4 High Performance, used to acquire, process, store, display and export d…Z-0274-2024

Questions about this company

How many recalls does Philips North America Llc have?
Recalert has 179 U.S. recalls on record for Philips North America Llc, published between April 5, 2017 and September 9, 2026.
Which agencies have handled Philips North America Llc recalls?
Philips North America Llc appears as the recalling firm in recalls from: FDA (179).

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