Product Recalls in Kentucky
Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,457 recalls have been distributed to Kentucky in the last 12 months.
Showing 28181–28200 of 28,748 recalls
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131F7J....
The Issue: The device is being recalled because the firm received multiple complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131F7P....
The Issue: The device is being recalled because the firm received multiple complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HF7P....
The Issue: The device is being recalled because the firm received multiple complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151HF7....
The Issue: The device is being recalled because the firm received multiple complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HF7J....
The Issue: The device is being recalled because the firm received multiple complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 141F7. For...
The Issue: The device is being recalled because the firm received multiple complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model TS057HF7....
The Issue: The device is being recalled because the firm received multiple complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 volume imaging ultrasound systems at software versions VA16C...
The Issue: In some cases, the system is unable to capture a clip or image during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS HIGH-FLOW AORTIC ARCH CANNULA: 6.5 MM (20 FR) 00 WITH 3/8" CONNECTOR...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 8.0 MM (24 FR) WITH 3/8" CONNECTOR Recalled...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 8.0 MM (24 FR) 00 WITH 3/8" CONNECTOR...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.