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. 2,646 recalls have been distributed to Kentucky in the last 12 months.
Showing 5261–5280 of 28,748 recalls
Recalled Item: 20IN (50.8CM) BRAIDED INJ LINE Recalled by Smiths Medical Asd Inc Due to...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6IN PRESSURE TUBING Recalled by Smiths Medical Asd Inc Due to There is a...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 11-12-13. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex 700PSI STOPCOCK W/ROTATOR Recalled by Smiths Medical Asd Inc Due to...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 16-17-18. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE ROTATOR WITH MALE LUER LOCK Recalled by Smiths Medical Asd Inc...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1050 STOPCOCK LEFT ROTATOR OFF HANDLE Recalled by Smiths Medical Asd Inc Due...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 48IN (121.9CM) INJ LINE ROTATING ADAPT (900psi) Recalled by Smiths Medical...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet G8 / G8E OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Prismalix OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet XTen OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Hanaulux 2006/ 2007 Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Hanaulux HLX2000 OR Light Systems Recalled by Getinge Usa Sales Inc...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Axcel / Axcel + OR Light Systems Recalled by Getinge Usa Sales Inc...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Hanaulux HLX3000 OR Light Systems Recalled by Getinge Usa Sales Inc...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Volista Recalled by Getinge Usa Sales Inc Due to A potential for a...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Equipment OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.