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. 2,672 recalls have been distributed to Kentucky in the last 12 months.
Showing 3221–3240 of 28,748 recalls
Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set APAC Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Pump Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pump 371 14F LT CMR Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 Set AU Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Platform (Endoscopy) Recalled by AURIS HEALTH INC Due to...
The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Platform (Urology) Recalled by AURIS HEALTH INC Due to...
The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAGNUM Disposable Core Tissue Biopsy Needle MN Recalled by Bard...
The Issue: Due to possible packaging damage (indentations/cuts) cause by manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Transcend Product Name: Transcend Singles Universal Body (UB)...
The Issue: Due to a manufacturing issue, red particulates present in the expressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Transcend Product Name: Transcend Econo Kit (UB) - Recalled by...
The Issue: Due to a manufacturing issue, red particulates present in the expressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Vit-l-escence Product Name: Vit-l-escence Singles A3...
The Issue: Due to a manufacturing issue, red particulates present in the expressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.