-
Patient Information Center iX 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
-
Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20… recall
FDA
· Philips North America Llc · Class II
-
CT 5300; Software Version Number: 4.5, 5.0, 5.1 recall
FDA
· Philips North America Llc · Class II
-
Incisive CT recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX850. Product Number: 866470 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX800. Product Number: 865240 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX750. Product Number: 866471 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX700. Product Number: 865241 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX600. Product Number: 865242 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX550. Product Number: 866066 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX500. Product Number: 866064 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX450. Product Number: 866062 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX400. Product Number: 866060 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX100. Product Number: 867033 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Multi-Measurement Module X3. Product Number: 867030 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Multi Measurement Server X2. Product Number: M3002A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP90. Product Number: M8010A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP80. Product Number: M8008A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP70. Product Number: M8007A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP60. Product Number: M8005A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP50. Product Number: M8004A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP40. Product Number: M8003A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP30. Product Number: M8002A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP20. Product Number: M8001A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP5. Product Number: M8105A recall
FDA
· Philips North America Llc · Class II
-
IntelliVue MP2. Product Number: M8102A recall
FDA
· Philips North America Llc · Class II
-
Cardiac Workstation 7000 recall
FDA
· Philips North America Llc · Class II
-
Cardiac Workstation 5000 recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Philips CT systems labeled as the following: 1… recall
FDA
· Philips North America Llc · Class II
-
Upgrade to MR 7700 Model Number ( recall
FDA
· Philips North America Llc · Class II
-
SmartPath to Ingenia Elition X Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for XR and 3.0T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for 3.0T Model Number ( recall
FDA
· Philips North America Llc · Class II
-
MR 7700 Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
MR 5300 Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Intera 3.0T Quasar Dual Model Number ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia Elition X Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia Elition S Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia Ambition X Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia Ambition S Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia 3.0T CX Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia 3.0T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T S Model Number ( recall
FDA
· Philips North America Llc · Class II
-
Ingenia 1.5T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Evolution Upgrade 3.0T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Evolution Upgrade 1.5T Model Numbers ( recall
FDA
· Philips North America Llc · Class II
-
Achieva XR recall
FDA
· Philips North America Llc · Class II
-
Achieva 3.0T recall
FDA
· Philips North America Llc · Class II
-
Spectral CT. Computed tomography X-ray system recall
FDA
· Philips North America Llc · Class II
-
SmartPath to dStream for 1.5T¿ recall
FDA
· Philips North America Llc · Class II