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. 2,602 recalls have been distributed to Kentucky in the last 12 months.
Showing 12661–12680 of 28,748 recalls
Recalled Item: ABL90 FLEX PLUS Recalled by Radiometer Medical ApS Due to The analyzers fail...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 630G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 640G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 620G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 670G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The...
The Issue: Four units of European version FreeStyle Comfort were distributed in the US,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Pin To Rod Coupling External Fixation System Hoffmann II Recalled by...
The Issue: Pin To Rod Coupling could not clamp the pin and rod as intended
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The products involved are DeWALT laser distance measurers Recalled by...
The Issue: The products are labeled as Class II lasers. However, the level of laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Durapore Advanced Recalled by 3M Company - Health Care Business Due to...
The Issue: While the product meets all safety and efficacy criteria, long term exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal KNEE BRACE Recalled by DeRoyal Industries Inc Due to The Warrior...
The Issue: The Warrior Recovery Knee Brace has the potential to come apart due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 8 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Safety Infusion System Y-type Blood Set Recalled by B. Braun...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 7 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 7.5 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.