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
September 9, 2026FDAPhilips Brilliance. Models: Brilliance iCT, Brilliance iCT Upgrades, Brilliance iCT SP. S…Z-3040-2026
September 9, 2026FDAPhilips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728…Z-3041-2026
September 9, 2026FDAPhilips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327, Ingenuity CT China 7…Z-3042-2026
September 9, 2026FDAPhilips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231, Brilliance CT 64…Z-3043-2026
August 26, 2026FDACardiac Workstation 7000. Product Number: 860441.Z-2956-2026
August 26, 2026FDACardiac Workstation 5000. Product Number: 860439.Z-2955-2026
July 1, 2026FDAPhilips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following syst…Z-2579-2026
July 1, 2026FDAPhilips Avalon Fetal Monitor, FM 30 Part numberM2703AZ-2523-2026
July 1, 2026FDAPhilips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703AZ-2522-2026
June 17, 2026FDADigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.Z-2354-2026
February 18, 2026FDASpectral CT; Product Code (REF): 728333;Z-1317-2026
February 18, 2026FDABrilliance iCT; Product Code (REF): 728306;Z-1315-2026
December 10, 2025FDACT 5300; Software Version Number: 4.5, 5.0, 5.1;Z-0882-2026
December 10, 2025FDAIntelliVue MP90. Product Number: M8010A.Z-0858-2026
December 10, 2025FDAIntelliVue Patient Monitor MX700. Product Number: 865241.Z-0867-2026
December 10, 2025FDAIntelliVue MP30. Product Number: M8002A.Z-0852-2026
December 10, 2025FDAIntelliVue Patient Monitor MX800. Product Number: 865240.Z-0869-2026
December 10, 2025FDAIntelliVue Patient Monitor MX500. Product Number: 866064.Z-0864-2026
December 10, 2025FDAIntelliVue Patient Monitor MX850. Product Number: 866470.Z-0870-2026
July 2, 2025FDASpectral CT. Computed tomography X-ray system.Z-2034-2025
May 28, 2025FDAProduct Name: Ingenia 3.0T CX; Model Number: 781271;Z-1800-2025
May 28, 2025FDAProduct Name: Ingenia 1.5T CX; Model Number: 781262;Z-1799-2025
May 28, 2025FDAProduct Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;Z-1805-2025
May 14, 2025FDAMicrostream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub …Z-1722-2025
April 30, 2025FDAVeradius Unity. Product Code 718132. The devices are used for radiological guidance and v…Z-1582-2025

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.
What was the most recent Philips North America Llc recall?
FDA recall Z-3040-2026, published September 9, 2026: Philips Brilliance. Models: Brilliance iCT, Brilliance iCT Upgrades, Brilliance iCT SP. Software 4.1.10.x Product Codes: 728306, 728305, 728311.
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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