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
May 10, 2023FDAPhilips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A…Z-1477-2023
December 14, 2022FDAPhilips SmartPath to Ingenia Elition X MR System, Model Numbers 782118, 782132, 782144Z-0461-2023
April 20, 2022FDAThe IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in the pa…Z-0926-2022
January 26, 2022FDAInfa-Therm Transport Mattress, Reference Number 989805616831 1015Z-0505-2022
October 20, 2021FDAPhilips, HeartStart HS1 OnSite Defibrillator, Model #'s: M5066A and M5067AZ-0081-2022
September 15, 2021FDAIngenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated for use as a di…Z-2414-2021
July 7, 2021FDAContinuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 882446 - V…Z-1988-2021
July 7, 2021FDAContinuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assemb…Z-1979-2021
July 7, 2021FDAContinuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728332 - I…Z-1985-2021
November 4, 2020FDAPhilips Sterilizable Defibrillator Paddles, Switched Internal Paddles, Model Numbers M474…Z-0284-2021
June 17, 2020FDAPhilips SureSigns VM1SpO2, C02, Rec, model no. 863266 - Product Usage: The SureSigns VM1 …Z-2337-2020
May 27, 2020FDAPhilips HeartStart XL Defibrillator/Monitor (Model number M4735A) - Product Usage: is for…Z-2053-2020
May 20, 2020FDAPhilips Zenition 70, System code 718133 - Product Usage: The devices are used for radiolo…Z-1933-2020
May 13, 2020FDAPhilips Brilliance iCT SP Computed Tomography X-Ray System; Model # 728311Z-1922-2020
May 13, 2020FDAPhilips Brilliance iCT Computed Tomography X-Ray System; Model # 728306; UDI #s (01)00884…Z-1921-2020
May 6, 2020FDAPhilips Azurion 7 M20 -XperGuide Software hosted in Interventional Workspot 1.5 when used…Z-1809-2020
April 8, 2020FDAExpression MR400 MRI Patient Monitoring System Model Number: 866185 Software version n…Z-1616-2020
March 25, 2020FDAUroDiagnost Eleva, system code 708033Z-1492-2020
March 25, 2020FDAIntegris Allura 9, system codes 722018 722021Z-1488-2020
March 25, 2020FDACardio Vascular-Allura Centron, system code 722400Z-1494-2020
March 4, 2020FDAPhilips DigiTrak XT Holter Recorder Software version number B.1 and C.2. The DigiTrak X…Z-1345-2020
September 18, 2019FDAHeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The HeartStart MRx …Z-2488-2019
July 17, 2019FDAPhilips HeartStart MRx devices in use with the M3539A AC Power Module: M3535A, M3536A, M…Z-1923-2019
June 12, 2019FDAIntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers All other countr…Z-1693-2019
May 22, 2019FDASureSigns VS3 NBP Temp, Product Number 863070. For monitoring the physiological paramete…Z-1318-2019

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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