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.
- Phillips 3.7V Rechargeable Li-Polymer Battery, Product #: 989803191341 - Product Usage: This battery is used in the Expression MR400 MRI Pa…
FDA Device · Class II · 2020-08-26 · Philips North America - Philips HeartStart MRx, Monitor/Defibrillators with model numbers M3535A, M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M353…
FDA Device · Class II · 2020-08-19 · Philips North America - IntelliVue MX700 patient monitor, model no. 865241
FDA Device · Class II · 2020-07-29 · Philips North America - IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 453564477391, 453564477401, 866173
FDA Device · Class II · 2020-07-29 · Philips North America - IntelliVue MX800 patient monitor, model no. 865240
FDA Device · Class II · 2020-07-29 · Philips North America - EasyDiagnost Eleva DRF, model no. 706050 - Product Usage: X-ray system, diagnostic, general-purpose
FDA Device · Class II · 2020-07-15 · Philips North America - Philips M3015A Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monitor (Model No. 867030) or a lntelliVue MM…
FDA Device · Class II · 2020-07-15 · Philips North America - Philips SureSigns VM1SpO2, C02, Rec, model no. 863266 - Product Usage: The SureSigns VM1 is a patient monitor that measures oxygen saturati…
FDA Device · Class II · 2020-06-17 · Philips North America - Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, r…
FDA Device · Class II · 2020-06-10 · Philips North America - Cardiovascular Monitoring Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration b…
FDA Device · Class II · 2020-06-10 · Philips North America - ProxiDiagnost N90, UDI 706100
FDA Device · Class II · 2020-06-10 · Philips North America - Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are an accessory to the compatible monitor/defibrillator Switchless:…
FDA Device · Class II · 2020-06-03 · Philips North America - Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product Usage: is for use in the hospital by qualified medical personne…
FDA Device · Class II · 2020-06-03 · Philips North America - Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A, M3536A, and M3536M - Product Usage: is for use for the termination of v…
FDA Device · Class II · 2020-06-03 · Philips North America - HeartStart MRx Processor Board PCA Replacement Kits 453563478461, a component of the Philips HeartStart MRx Monitorl/Defibrillator - Produc…
FDA Device · Class II · 2020-05-27 · Philips North America - Philips HeartStart XL Defibrillator/Monitor (Model number M4735A) - Product Usage: is for use in the hospital by qualified medical personne…
FDA Device · Class II · 2020-05-27 · Philips North America - Philips Zenition 50, System code 718096 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic…
FDA Device · Class II · 2020-05-20 · Philips North America - Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic…
FDA Device · Class II · 2020-05-20 · Philips North America - Philips Brilliance iCT SP Computed Tomography X-Ray System
FDA Device · Class II · 2020-05-13 · Philips North America - Philips Brilliance IQon Spectral CT, Computed Tomography X-Ray System
FDA Device · Class II · 2020-05-13 · Philips North America - Philips Brilliance iCT Computed Tomography X-Ray System
FDA Device · Class II · 2020-05-13 · Philips North America - Phillips Azurion 7 M20, Angiographic X-Ray System Code 722079 Image guidance in diagnostic, interventional and minimally invasive surgery p…
FDA Device · Class II · 2020-05-06 · Philips North America - Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography
FDA Device · Class II · 2020-05-06 · Philips North America - Philips Azurion 7 M20 -XperGuide Software hosted in Interventional Workspot 1.5 when used with the Azurion R2.0 system Interventional fluor…
FDA Device · Class II · 2020-05-06 · Philips North America - Expression MR400 MRI Patient Monitoring System Model Number: 866185 Software version number: 01.03.00, 01.04.00, 01.05.00, and 01.07.00 - P…
FDA Device · Class II · 2020-04-08 · Philips North America - UroDiagnost Eleva, system code 708033
FDA Device · Class II · 2020-03-25 · Philips North America - MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038
FDA Device · Class II · 2020-03-25 · Philips North America - Integris Allura 15 & 12, monoplane (system code 722043) and biplane (system code 722044)
FDA Device · Class II · 2020-03-25 · Philips North America - HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536…
FDA Device · Class II · 2020-03-25 · Philips North America - Cardio Vascular-Allura Centron, system code 722400
FDA Device · Class II · 2020-03-25 · Philips North America - Integris Allura 9, system codes 722018 722021
FDA Device · Class II · 2020-03-25 · Philips North America - Allura Exper FD Series
FDA Device · Class II · 2020-03-25 · Philips North America - OmniDiagnost Eleva System codes 708028 708027
FDA Device · Class II · 2020-03-25 · Philips North America - Poly G Integris H5000, System code 72246
FDA Device · Class II · 2020-03-25 · Philips North America - Allura CV20, system code 722031
FDA Device · Class II · 2020-03-25 · Philips North America - Ambulance Parameter Extension (APE) kit M4758A, an accessory to the Philips HeartStart MRx Monitor/Defibrillator - Product Usage: is intend…
FDA Device · Class II · 2020-03-04 · Philips North America - Philips DigiTrak XT Holter Recorder Software version number B.1 and C.2. The DigiTrak XT Recorder is available in four different configurat…
FDA Device · Class II · 2020-03-04 · Philips North America - Philips HeartStart HS1 Onsite (Model M5066A) and HSI Home (Model M5068A) AED, Model 861304, HSI codeRev: E.03.063
FDA Device · Class II · 2020-02-26 · Philips North America - Philips HeartStart FRx AED, Model 861304, FRx codeRev: E.02.017
FDA Device · Class II · 2020-02-26 · Philips North America - VesselNavigator application used with Philips Azurion (Azurion 7 Series) Software R1.2 and R2.0, and Philips Allura Xper R9, upgraded to Az…
FDA Device · Class II · 2020-02-19 · Philips North America - HeartStart XL+ Defibrillator/Monitor, Model 861290
FDA Device · Class II · 2019-12-11 · Philips North America - HeartStart XL+ Defibrillator/Monitor, Model 861290
FDA Device · Class II · 2019-11-27 · Philips North America - Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
FDA Device · Class II · 2019-10-02 · Philips North America - IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The affected product is a 74 foot (22.6m) combined coax and unshielded tw…
FDA Device · Class II · 2019-09-25 · Philips North America - HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The HeartStart MRx is a lightweight, portable external defibrillator,…
FDA Device · Class II · 2019-09-18 · Philips North America - Philips 5-Lead Set, Disposable, Bedside, AAMI Model # 989803173131 Product Usage: Philips Single-Patient-Use ECG lead sets for bedside moni…
FDA Device · Class II · 2019-09-18 · Philips North America - Philips Azurion systems with software version R1.2 -Interventional Fluoroscopic X-ray system as follows: Azurion 3 M12, Azurion 3 M15, Azur…
FDA Device · Class II · 2019-08-14 · Philips North America - Philips HeartStart MRx devices in use with the M3539A AC Power Module: M3535A, M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5,…
FDA Device · Class II · 2019-07-17 · Philips North America - Philips IntelliBridge System configured with a regional setting which uses a comma for a decimal separator: 866417 IntelliBridge System C.0…
FDA Device · Class III · 2019-06-19 · Philips North America - Philips Patient Information Center iX configured with a regional setting which uses a comma for a decimal separator: 866389 Patient Informa…
FDA Device · Class III · 2019-06-19 · Philips North America