Philips North America Llc

Frequent Recalls

10

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-06-17 to 2026-09-09

Date	Source	Product	Brand	Severity	Units
2026-09-09	FDA Device	FDA Recall: Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231, Brilliance CT 64 Upgrades P	Philips North America Llc	Class II	N/A
2026-09-09	FDA Device	FDA Recall: Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327, Ingenuity CT China 728324, Ing	Philips North America Llc	Class II	N/A
2026-09-09	FDA Device	FDA Recall: Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Softwa	Philips North America Llc	Class II	N/A
2026-09-09	FDA Device	FDA Recall: Philips Brilliance. Models: Brilliance iCT, Brilliance iCT Upgrades, Brilliance iCT SP. Software 4.1	Philips North America Llc	Class II	N/A
2026-08-26	FDA Device	FDA Recall: Cardiac Workstation 7000. Product Number: 860441.	Philips North America Llc	Class II	N/A
2026-08-26	FDA Device	FDA Recall: Cardiac Workstation 5000. Product Number: 860439.	Philips North America Llc	Class II	N/A
2026-07-01	FDA Device	FDA Recall: Philips Avalon Fetal Monitor, FM 30 Part numberM2703A	Philips North America Llc	Class II	N/A
2026-07-01	FDA Device	FDA Recall: Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A	Philips North America Llc	Class II	N/A
2026-07-01	FDA Device	FDA Recall: Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descript	Philips North America Llc	Class II	N/A
2026-06-17	FDA Device	FDA Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.	Philips North America Llc	Class II	N/A

Philips North America Llc Recalls | WatchRecall