Brand

Philips North America, Llc Recalls

260 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Philips North America, Llc.

260Total Recalls
34Critical
46.6MUnits Affected
Jan 7, 2026Most Recent
All Recalls

Every Philips North America, Llc Recall

Sorted by most recent. Click any recall for full details.

260 recalls
High RiskFDA
Philips North America Llc
Brilliance iCT; Product Code (REF): 728306;
Medical Devices·47 affected·Jan 7, 2026
High RiskFDA
Philips North America Llc
Spectral CT; Product Code (REF): 728333;
Medical Devices·283 affected·Jan 7, 2026
High RiskFDA
Philips North America Llc
IQon Spectral CT; Product Code (REF): 728332;
Medical Devices·52 affected·Jan 7, 2026
High RiskFDA
Philips North America Llc
IntelliVue MP90. Product Number: M8010A.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue MP30. Product Number: M8002A.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue Patient Monitor MX800. Product Number: 865240.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue Patient Monitor MX700. Product Number: 865241.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue Patient Monitor MX500. Product Number: 866064.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue Patient Monitor MX850. Product Number: 866470.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue MP2. Product Number: M8102A.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue MP50. Product Number: M8004A.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue MP80. Product Number: M8008A.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue Patient Monitor MX100. Product Number: 867033.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue MP40. Product Number: M8003A.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue Multi Measurement Server X2. Product Number: M3002A.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
IntelliVue MP60. Product Number: M8005A.
Medical Devices·1,913,441 affected·Oct 31, 2025
High RiskFDA
Philips North America Llc
CT 5300; Software Version Number: 4.5, 5.0, 5.1;
Medical Devices·6 affected·Oct 29, 2025
High RiskFDA
Philips North America Llc
Incisive CT; Software Version Number: 4.5, 5.0, 5.1;
Medical Devices·2,341 affected·Oct 29, 2025
High RiskFDA
Philips North America Llc
Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.
Medical Devices·210 affected·Aug 13, 2025
High RiskFDA
Philips North America Llc
Philips CT systems labeled as the following: 1. IQon Spectral CT, Model Number: 728332.
Medical Devices·81 affected·Aug 13, 2025
High RiskFDA
Philips North America Llc
Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Oncology, Model Numbe...
Medical Devices·33 affected·Aug 13, 2025
High RiskFDA
Philips North America Llc
Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.
Medical Devices·3 affected·Aug 13, 2025
High RiskFDA
Philips North America Llc
Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307.
Medical Devices·6 affected·Aug 13, 2025
High RiskFDA
Philips North America Llc
Philips CT systems labeled as the following: 1. Brilliance 16 Power, Model Number: 728240. 2. Brilliance CT 16 Slice, Model Number...
Medical Devices·73 affected·Aug 13, 2025
High RiskFDA
Philips North America Llc
Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64 Channel, Model...
Medical Devices·181 affected·Aug 13, 2025
High RiskFDA
Philips North America Llc
Spectral CT. Computed tomography X-ray system.
Medical Devices·370 affected·May 29, 2025
High RiskFDA
Philips North America Llc
Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
Medical Devices·28 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: Ingenia 3.0T CX; Model Number: 781271;
Medical Devices·37 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: Ingenia 1.5T CX; Model Number: 781262;
Medical Devices·9 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;
Medical Devices·72 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136;
Medical Devices·198 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;
Medical Devices·193 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: Ingenia 1.5T S; Model Number: 781347;
Medical Devices·2 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: SmartPath to dStream for 3.0T; Model Number: 782145
Medical Devices·12 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138;
Medical Devices·300 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137;
Medical Devices·65 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;
Medical Devices·16 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;
Medical Devices·152 affected·May 13, 2025
High RiskFDA
Philips North America Llc
Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm L...
Medical Devices·486,631 affected·Apr 7, 2025
High RiskFDA
Philips North America Llc
Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
Medical Devices·630 affected·Apr 1, 2025
High RiskFDA
Philips North America Llc
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
Diagnostic Devices·83 affected·Mar 10, 2025
High RiskFDA
Philips North America Llc
Zenition 70. Product Code 718133. The devices are used for radiological guidance and visualization during diagnostic, interventional and ...
Surgical Devices·0 affected·Feb 25, 2025
High RiskFDA
Philips North America Llc
Veradius Unity. Product Code 718132. The devices are used for radiological guidance and visualization during diagnostic, interventional a...
Surgical Devices·0 affected·Feb 25, 2025
High RiskFDA
Philips North America Llc
Zenition 50. Product Code 718096. The devices are used for radiological guidance and visualization during diagnostic, interventional and...
Surgical Devices·0 affected·Feb 25, 2025
High RiskFDA
Philips North America Llc
IntelliVue Patient Monitor MX400. Model Number: 866060
Medical Devices·28 affected·Jan 15, 2025
High RiskFDA
Philips North America Llc
IntelliVue Patient Monitor MX450. Model Number: 866062
Medical Devices·98 affected·Jan 15, 2025
High RiskFDA
Philips North America Llc
IntelliVue Patient Monitor MX550. Model Number: 866066
Medical Devices·74 affected·Jan 15, 2025
High RiskFDA
Philips North America Llc
IntelliVue Patient Monitor MX500. Model Number: 866064
Medical Devices·45 affected·Jan 15, 2025