Philips North America recalls
Philips North America appears in 532 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.
- CombiDiagnost R90 R1.1
FDA Device · Class II · 2023-05-24 · Philips North America - Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-functional general radiography and fluorosco…
FDA Device · Class II · 2023-05-10 · Philips North America - Philips DigitalDiagnost C50 -intended for use in generating radiographic images of human anatomy Model Number : 712201
FDA Device · Class II · 2023-04-19 · Philips North America - CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 709030 and 709031
FDA Device · Class II · 2023-04-19 · Philips North America - DigitalDiagnost C50 1.1-intended for use in generating radiographic images of human anatomy Model Number : 712204
FDA Device · Class II · 2023-04-19 · Philips North America - ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
FDA Device · Class II · 2023-04-19 · Philips North America - Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during labor
FDA Device · Class II · 2023-01-18 · Philips North America - Philips SmartPath to Ingenia Elition X MR System, Model Numbers 782118, 782132, 782144
FDA Device · Class II · 2022-12-14 · Philips North America - Philips Ingenia Elition X MR System, Model Numbers 781358, 782107, 782119, 782136
FDA Device · Class II · 2022-12-14 · Philips North America - Philips Ingenia Elition S MR System, Model Numbers 781357, 782106, 782137
FDA Device · Class II · 2022-12-14 · Philips North America - Philips MR 7700 System, Model Number 782120
FDA Device · Class II · 2022-12-14 · Philips North America - Philips Upgrade to MR 7700 System, Model Number 782130
FDA Device · Class II · 2022-12-14 · Philips North America - MR Patient Care Portal 5000 (Desktop Unit), Model Number 453564792561 This is a component of product number 866162
FDA Device · Class II · 2022-10-12 · Philips North America - DigitalDiagnost C50 1.1
FDA Device · Class II · 2022-09-07 · Philips North America - Philips Hemodynamic Application, Model Number 722463, Software Version Number: R1.2.2 and R1.2.3. For visualization and analysis of patient…
FDA Device · Class II · 2022-05-18 · Philips North America - The IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in the packaging for the following product model #s: 21075A…
FDA Device · Class II · 2022-04-20 · Philips North America - Philips, REF M5071A, Adult
FDA Device · Class II · 2022-04-13 · Philips North America - Philips Allura (Model Numbers 722010, 722012, 722026, 722027, 722028, 722029, 722035) and Philips Azurion (Model Numbers 722063, 722064, 72…
FDA Device · Class II · 2022-04-13 · Philips North America - Philips, REF M5072A, INFANT/CHILD - SMART PADS CARTRIDGE (0-8 YEARS). Smart PADS CARTRIDGE , (0-8 YEARS) <55 lbs/25 kg, CE 0123, NON-STERIL…
FDA Device · Class II · 2022-04-13 · Philips North America - 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