-
Intera Achieva 1.5T Pulsar recall
FDA
· Philips North America Llc · Class II
-
Intera 1.5T Omni/Stellar recall
FDA
· Philips North America Llc · Class II
-
Intera 1.5T Master/Nova Product Number: 781106 recall
FDA
· Philips North America Llc · Class II
-
Intera 1.5T Explorer/Nova Dual Product Number: 781108 recall
FDA
· Philips North America Llc · Class II
-
Intera 1.5T Achieva Nova-Dual Product Number: 781173 recall
FDA
· Philips North America Llc · Class II
-
Intera 1.5T Achieva Nova Product Number: 781172 recall
FDA
· Philips North America Llc · Class II
-
Intera 1.5T Achieva IT Nova Product Number: 781175 recall
FDA
· Philips North America Llc · Class II
-
Achieva XR Product Numbers: (1) 781153, (2) 781253 recall
FDA
· Philips North America Llc · Class II
-
MR 7700; Model Numbers: (1) 782120, (2) 782153 recall
FDA
· Philips North America Llc · Class II
-
MR 5300; Model Numbers: (1) 782110, (2) 782152 recall
FDA
· Philips North America Llc · Class II
-
Ingenia Elition X recall
FDA
· Philips North America Llc · Class II
-
Ingenia Elition S recall
FDA
· Philips North America Llc · Class II
-
Ingenia Ambition X recall
FDA
· Philips North America Llc · Class II
-
Ingenia 3.0T CX recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T CX recall
FDA
· Philips North America Llc · Class II
-
Ingenia Ambition S recall
FDA
· Philips North America Llc · Class II
-
Ingenia 3.0T recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T S recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T recall
FDA
· Philips North America Llc · Class II
-
Evolution Upgrade 3.0T recall
FDA
· Philips North America Llc · Class II
-
Evolution Upgrade 1.5T recall
FDA
· Philips North America Llc · Class II
-
Upgrade to MR 7700 recall
FDA
· Philips North America Llc · Class II
-
SmartPath to Ingenia Elition X recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for XR and 3.0T recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for 3.0T recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for 1.5T recall
FDA
· Philips North America Llc · Class II
-
Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as… recall
FDA
· Philips North America Llc · Class II
-
Philips Brilliance CT Big Bore, Software Version 4.8.0.10430… recall
FDA
· Philips North America Llc · Class II
-
Veradius Unity recall
FDA
· Philips North America Llc · Class II
-
Zenition 70. Product Code 718133. The devices are used for radiological… recall
FDA
· Philips North America Llc · Class II
-
Zenition 50. Product Code 718096. The devices are used for radiological… recall
FDA
· Philips North America Llc · Class II
-
Philips DXR System, DuraDiagnost Rel recall
FDA
· Philips North America Llc · Class II
-
Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX550. Model Number: 866066 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX500. Model Number: 866064 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX450. Model Number: 866062 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX400. Model Number: 866060 recall
FDA
· Philips North America Llc · Class II
-
IntelliBridge EC10 Module recall
FDA
· Philips North America Llc · Class II
-
Philips Smart-Hopping 2.0 AP 1.4 GHz recall
FDA
· Philips North America Llc · Class II
-
Spectral CT and Spectral CT Plus recall
FDA
· Philips North America Llc · Class II
-
ST SENSE Breast Dx Coil recall
FDA
· Philips North America Llc · Class II
-
ST SENSE Breast Coil recall
FDA
· Philips North America Llc · Class II
-
SENSE Breast Coil 3.0T 7ch recall
FDA
· Philips North America Llc · Class II
-
SENSE Breast Coil recall
FDA
· Philips North America Llc · Class II
-
Mammotrak Interventional Coil 3.0T recall
FDA
· Philips North America Llc · Class II
-
Mammotrak Diagnostic Coil 3.0T recall
FDA
· Philips North America Llc · Class II
-
Mammotrak Interventional Coil 1.5T recall
FDA
· Philips North America Llc · Class II
-
Mammotrak Diagnostic Coil 1.5T recall
FDA
· Philips North America Llc · Class II
-
dS Breast 7ch 3.0T recall
FDA
· Philips North America Llc · Class II
-
dS Breast 7ch 1.5T recall
FDA
· Philips North America Llc · Class II
-
dS Breast 16ch 3.0T recall
FDA
· Philips North America Llc · Class II
-
dS Breast 16ch 1.5T recall
FDA
· Philips North America Llc · Class II
-
Achieva TX Interventional Coil 3.0T recall
FDA
· Philips North America Llc · Class II
-
Patient Information Center iX, Product Code 866386… recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version… recall
FDA
· Philips North America Llc · Class II
-
DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX… recall
FDA
· Philips North America Llc · Class II
-
IntelliVue G7m Anesthesia Gas Module, Product Number 866173 recall
FDA
· Philips North America Llc · Class II