Philips North America recalls
Philips North America appears in 563 official U.S. recall notices indexed by RecallRadar.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722…
FDA Device · Class II · 2022-03-16 · Philips North America - Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an exten…
FDA Device · Class II · 2022-03-16 · Philips North America - eCareManager version 4.2.1, eCareManager version 4.3.2, eCareManager version 4.3.3, eCareManager version 4.5.1, eCareManager version 4.5.2,…
FDA Device · Class II · 2022-02-09 · Philips North America - Medichoice Infant Heel Warmer, Reference # 989805643721 1079906
FDA Device · Class II · 2022-01-26 · Philips North America - Infa-Therm Transport Mattress, Reference Number 989805616831 1015
FDA Device · Class II · 2022-01-26 · Philips North America - Cardinal Infant Heel Warmer, Reference # 989805617251 11470-010T
FDA Device · Class II · 2022-01-26 · Philips North America - Heel Snuggler, Reference # 989805603411 99047
FDA Device · Class II · 2022-01-26 · Philips North America - Infant Heel Warmers w/strap, Reference # 989805603201 1223
FDA Device · Class II · 2022-01-26 · Philips North America - Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2 with LUC configuration start-up issue
FDA Device · Class II · 2022-01-19 · Philips North America - Wireless Footswtich used with the following Philips Allura Xper and Azurion Interventional Fluoroscopic X-ray System . Model Number: 722001…
FDA Device · Class II · 2022-01-19 · Philips North America - Philips Allura Xper FD series with Software Version Number: 2.1.x- intended for Vascular, cardiovascular and neurovascular imaging applicat…
FDA Device · Class II · 2021-12-29 · Philips North America - BV Endura with Software Release 2.3- A mobile, diagnostic X-ray image acquisition and viewing system
FDA Device · Class II · 2021-12-15 · Philips North America - BV Pulsera with Software Release 2.3-A mobile, diagnostic X-ray image acquisition and viewing system
FDA Device · Class II · 2021-12-15 · Philips North America - Veradius Unity with Software Release 2.1- Amobile, diagnostic X-ray imaging and viewing system. . Model Number: 718132
FDA Device · Class II · 2021-12-15 · Philips North America - Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini TF 64 System Number: 882471 Continuous CT (CCT) is a CT or PET/CT…
FDA Device · Class II · 2021-12-01 · Philips North America - Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - CT Vision ACQSIM CT System Number: 728209 Continuous CT (CCT) is a CT or…
FDA Device · Class II · 2021-12-01 · Philips North America - Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini GXL 16 Slice System Number: 882410 Continuous CT (CCT) is a CT or…
FDA Device · Class II · 2021-12-01 · Philips North America - Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - TruFlight Select PET/CT System Number: 882438 Continuous CT (CCT) is a C…
FDA Device · Class II · 2021-12-01 · Philips North America - Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini TF 16 System Number: 882470 Continuous CT (CCT) is a CT or PET/CT…
FDA Device · Class II · 2021-12-01 · Philips North America - Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model numbers 722063, 722064, 722067, 722068, 722078, 722…
FDA Device · Class II · 2021-11-17 · Philips North America - Philips, HeartStart FRx + Defibrillator, Model # Model #s: 861304
FDA Device · Class II · 2021-10-20 · Philips North America - Philips, HeartStart HS1 OnSite Defibrillator, Model #'s: M5066A and M5067A
FDA Device · Class II · 2021-10-20 · Philips North America - Philips, HeartStart HS1 Home Defibrillator, Model # Model number: M5068A
FDA Device · Class II · 2021-10-20 · Philips North America - Philips, HeartStart FR2 + Defibrillator, Model # M3860A and M3861A
FDA Device · Class II · 2021-10-20 · Philips North America - The Azurion series (within the limits of the used Operation Room table) are intended for use to perform: "Image guidance in diagnostic, int…
FDA Device · Class II · 2021-09-22 · Philips North America - The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular imaging applications,…
FDA Device · Class II · 2021-09-22 · Philips North America - The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular imaging applications,…
FDA Device · Class II · 2021-09-22 · Philips North America - Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia Elition X-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - SmartPath to dStream for 1.5T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia Ambition X- Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia 1.5T S-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - SmartPath to dStream for XR and 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Philips, HEARTSTART, INFANT/CHILD - SMART PADS CARTRIDGE, REF: M5072A, (0-8 YEARS)< 55 lbs / 25 kg, CE 0123, NON-STERILE, Rx only, UDI: (01…
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia Ambition S-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia Elition S-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia 3.0T CX-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-15 · Philips North America - Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-01 · Philips North America - Ingenia 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-01 · Philips North America - Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-01 · Philips North America - Ingenia CX 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-01 · Philips North America - Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-01 · Philips North America - Ingenia Elition S-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-01 · Philips North America - Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device
FDA Device · Class II · 2021-09-01 · Philips North America - Model 728321/728323 CT5000 Ingenuity Plus/Pro/Premium-Computed Tomography X-ray system
FDA Device · Class II · 2021-08-25 · Philips North America - 728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance iCT Upgrades
FDA Device · Class II · 2021-08-25 · Philips North America - 728332 IQon Spectral CT-Computed Tomography X-ray system
FDA Device · Class II · 2021-08-25 · Philips North America