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. 1,099 recalls have been distributed to Kentucky in the last 12 months.
Showing 9261–9280 of 51,386 recalls
Recalled Item: Driver Instrument Recalled by Boston Scientific Neuromodulation Corporation...
The Issue: Pending update to indirect decompression system instructions for use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline O.R. Scissors Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: The scissors were manufactured without a tip protector resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Icelock 125 Ratchet Recalled by Ossur H / F Due to A mechanical lock used to...
The Issue: A mechanical lock used to connect and release a locking liner into a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial Recalled by Revive Rx...
The Issue: Sub-potent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Julie's Real JR Bar Dark Chocolate Grain-Free Granola Bar Recalled by...
The Issue: Possible presence of foreign material (metal)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Julie's Real JR Bar Cinnamon Vanilla Bean Grain-Free Granola Bar Recalled by...
The Issue: Possible presence of foreign material (metal)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CRTD VIVA QUAD XT CUST PARY GOLD Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-VR DVBB1D4 EVERA XT DF4 US Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRTD DTMB2Q1 AMPLIA MRI QUAD OUS DF1 Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-VR DVFC3D1 VISIA AF MRI S OUS/US DF1 Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-VR DVBC3D1 EVERA S IS1/DF1 GLOB Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-DR DDMB2D4 EVERA MRI XT IS-1/DF4 INT Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-DR DDBB1D1 EVERA XT IS1/DF1 US Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRTD COBALT XT HF MRI IS1 DF4 Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-DR DDBB1D4 EVERA XT IS1/DF4 US Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD CROME DR MRI IS1 DF4 Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.