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. 1,865 recalls have been distributed to Kentucky in the last 12 months.
Showing 27301–27320 of 51,386 recalls
Recalled Item: Flucanazole Injection Recalled by Renaissance Lakewood, LLC Due to...
The Issue: Superpotent and Failed Stability Specifications; out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fabius Tiro Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius GS Premium Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius MRI Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius Tiro M Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to Several complaints were...
The Issue: Several complaints were received for invalid calibration with low calibrator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic...
The Issue: During assembly, an SRS Humeral Distal Body implant failed to engage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neonatal PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Kit Recalled by Vygon U.S.A. Due to Potential friction holes may affect...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Barrier Insertion Tray Recalled by Vygon U.S.A. Due to Potential...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes may...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL ER...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lemongrass Facial Polish with Oats Recalled by Plant Devas Inc Due to FDA...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rose Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of Colors...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blemish Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clay Mask Kit Recalled by Plant Devas Inc Due to FDA Office of Colors and...
The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...
Recommended Action: Do not consume. Return to store for a refund or discard.