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. 2,672 recalls have been distributed to Kentucky in the last 12 months.
Showing 981–1000 of 51,386 recalls
Recalled Item: Opdualag (nivolumab and relatlimab-rmbw) injection Recalled by Bristol-Myers...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CareLink Clinic Recalled by Medtronic MiniMed, Inc. Due to Software error...
The Issue: Software error causing incorrect data to be displayed on the 24-hour Sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow PRUTest Platelet Reactivity Test UDI-DI code: 10711234150078...
The Issue: Due to an device without a premarket clearance being incorrectly package and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SILINTAN 25/pills Recalled by ANTHONY TRINH, 123Herbals LLC Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NIACIN Extended-Release Tablets Recalled by Golden State Medical Supply Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Klarity-C Drops (Cyclosporine) 0.1% Recalled by Imprimis NJOF, LLC Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System....
The Issue: Potential for anesthesia leakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Isoflurane (ISO) V90 Electronic Vaporizer with the A9 Anesthesia System....
The Issue: Potential for anesthesia leakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HR-ACT (High Range Activated Clotting Time Cartridges) Recalled by...
The Issue: Medtronic personnel observed trace amounts of dry blood on the external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONARCH Bronchoscope. Model Number: MBR-000211-B Recalled by Auris Health,...
The Issue: Potential that product was leak tested with equipment outside of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Town Food Service EQ CO Inc. brand Aluminum Sauce Pans in 1QT Recalled by...
The Issue: Product found to contain leachable lead levels.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acetaminophen 500mg Caffeine 65mg caplets Recalled by Aero Healthcare Due to...
The Issue: Labeling: Label Mix-up. This issue affects the outer box labeling only. The...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Emdogain Recalled by Straumann USA LLC Due to The possibility for this...
The Issue: The possibility for this product that is intended for demonstration purposes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS - InteleConnect / TechPortal Recalled by INTELERAD MEDICAL...
The Issue: Software application that receives digital images and data to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris infusion Pump Module 8100 Recalled by CareFusion 303, Inc. Due to...
The Issue: If infusion pump is dropped or severely jarred this may damage the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EZDilate Nephrostomy Balloon Catheter and Inflation Device Kit...
The Issue: Device kits contained an incorrectly sized 4mm x 4cm urinary tract balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...
The Issue: A potential issue with the seal integrity of header bag packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.