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. 1,886 recalls have been distributed to Kentucky in the last 12 months.
Showing 24001–24020 of 51,386 recalls
Recalled Item: Ingenia Ambition X Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR-OR 1.5T Recalled by Philips Medical Systems Nederlands Due to There is a...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T for PET Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama 1.0T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 0.5T Standard Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T High Performance Recalled by Philips Medical Systems Nederlands...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P) 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia WT(P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.