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.

• DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images
  FDA Device · Class II · 2023-11-15 · Philips North America
• DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images
  FDA Device · Class II · 2023-11-15 · Philips North America
• Azurion IGTS Fixed Systems
  FDA Device · Class II · 2023-11-15 · Philips North America
• CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system
  FDA Device · Class II · 2023-11-15 · Philips North America
• EasyDiagnost Eleva DRF, Release 5, used to acquire, process, store, display and export digital radiographic images
  FDA Device · Class II · 2023-11-15 · Philips North America
• Zenition 50 & 70 Mobile Surgery C-arm
  FDA Device · Class II · 2023-11-15 · Philips North America
• ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system
  FDA Device · Class II · 2023-11-15 · Philips North America
• DigitalDiagnost C90 High Performance, used to acquire, process, store, display and export digital radiographic images
  FDA Device · Class II · 2023-11-15 · Philips North America
• Allura Xper IGTS Fixed Systems
  FDA Device · Class II · 2023-11-15 · Philips North America
• Integris-Allura IGTS Fixed Systems
  FDA Device · Class II · 2023-11-15 · Philips North America
• EarlyVue VS30 Vital Signs Monitor, utilizing E01 (Oridion Microstream sidestream etCO2) and R21 (Masimo Rainbow RRa) simultaneously, Produc…
  FDA Device · Class II · 2023-10-11 · Philips North America
• EarlyVue VS30 Vitals Monitor, utilizing E01 (Oridion Microstream sidestream etCO2) and R21 (Masimo Rainbow RRa) simultaneously, Product Cod…
  FDA Device · Class II · 2023-10-11 · Philips North America
• Patient Information Center iX with Software Version Number 4.x in the following: (1) Patient Information Center iX Product Number: 866389;…
  FDA Device · Class II · 2023-09-27 · Philips North America
• Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106
  FDA Device · Class II · 2023-08-16 · Philips North America
• Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
  FDA Device · Class II · 2023-08-16 · Philips North America
• Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106
  FDA Device · Class II · 2023-08-16 · Philips North America
• Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
  FDA Device · Class II · 2023-08-16 · Philips North America
• MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
  FDA Device · Class II · 2023-08-16 · Philips North America
• MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
  FDA Device · Class II · 2023-08-16 · Philips North America
• Incisive CT Plus-Computed Tomography X-Ray System Model: 728149
  FDA Device · Class II · 2023-08-09 · Philips North America
• Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146
  FDA Device · Class II · 2023-08-09 · Philips North America
• Incisive CT Power (China)-Computed Tomography X-Ray System Model: 728148
  FDA Device · Class II · 2023-08-09 · Philips North America
• Incisive CT-Computed Tomography X-Ray System Model: 728143
  FDA Device · Class II · 2023-08-09 · Philips North America
• DigitalDiagnost C90, Model No. 712034 and 712035
  FDA Device · Class II · 2023-07-05 · Philips North America
• EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01 Product Number: 863359
  FDA Device · Class II · 2023-06-07 · Philips North America
• EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01 Product Number: 863380
  FDA Device · Class II · 2023-06-07 · Philips North America
• CombiDiagnost R90 R.1.0
  FDA Device · Class II · 2023-05-24 · Philips North America
• ProxiDiagnost N90 R.1.0
  FDA Device · Class II · 2023-05-24 · Philips North America
• Spectral CT 7500 Computed Tomography X-Ray System, Model Number 728333
  FDA Device · Class II · 2023-05-24 · Philips North America
• Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813
  FDA Device · Class II · 2023-05-24 · Philips North America
• Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814
  FDA Device · Class II · 2023-05-24 · Philips North America
• 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