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. 1,137 recalls have been distributed to Kentucky in the last 12 months.
Showing 961–980 of 51,386 recalls
Recalled Item: BD Kiestra" Isolate Suspension Cuvette Array Recalled by Becton Dickinson &...
The Issue: The 2D barcodes on these cuvettes contain formatting errors that prevent the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strawberry Cheesecake Ice Cream with graham crackers swirl Recalled by Ice...
The Issue: Foreign material fragments consisting of aluminum foil and packaging...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bakery Graham Pieces Recalled by Ice Cream Factory, LLC Due to Foreign...
The Issue: Foreign material fragments consisting of aluminum foil and packaging...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...
The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...
The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...
The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire Respiratory Panel 2.1 Recalled by BioFire Diagnostics, LLC Due to...
The Issue: Due to unintended movement of pouch chemistry, nucleic acid test may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TYLENOL Recalled by Kenvue Brands LLC Due to Defective Container
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.