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. 1,008 recalls have been distributed to Kentucky in the last 12 months.
Showing 25161–25180 of 51,386 recalls
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite 25 GA Vit Cutter Recalled by Bausch & Lomb Inc...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy 3 Implant Recalled by Implant Direct Sybron...
The Issue: Two units in distribution were found to be mislabeled on the vial cap with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ColoCARE Recalled by Helena Laboratories, Corp. Due to The positive control...
The Issue: The positive control on some tests of the lots did not appropriately react...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ColoCARE Recalled by Helena Laboratories, Corp. Due to The positive control...
The Issue: The positive control on some tests of the lots did not appropriately react...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart Infant/Child SMART Pads Cartridge Recalled by Philips...
The Issue: The recall is being initiated due to incorrect age range labeling (8+ yrs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Ophthalmic Solution 0.05% Recalled by Akorn, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications:out-of-specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: Out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: Out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Hyclate USP Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due...
The Issue: Failed Dissolution Specifications: manufacturer West-Ward Pharm Corp....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ImplantDirect simply RePlant Implant Recalled by Implant Direct Sybron...
The Issue: The incorrect device was packaged in the vial.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minimed Model 500 Remote Control (MMT-500 Recalled by Medtronic Inc. Due to...
The Issue: There is a potential security vulnerability related to the use of the remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.