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 2401–2420 of 28,748 recalls
Recalled Item: Karl Storz - Endoskope - - Optical Biopsy and Grasping Forceps Recalled by...
The Issue: Due to failure of manual cleaning validation, biopsy and grasping forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Heparin Calibrators Recalled by Instrumentation Laboratory Due to...
The Issue: Control indicating lower than expected quality control (QC) results and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus MAJ-891 Forceps/Irrigation Plug (Isolated Type). Model/Catalog...
The Issue: Potential for inadvertent retention of biomaterial when the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide Recalled by Tornier...
The Issue: The Pin Guide is being recalled because the metal tube may disassemble from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to 5R 16MM...
The Issue: 5R 16MM knee tibial insert package may contain knee tibial insert 3R 14MM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitoring Service Application (MSA). Software to process Recalled by...
The Issue: Not all Electrocardiogram (ECG) events received July 2022-July 2024 were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...
The Issue: There is over-molding that stabilizes the connection between the cable and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...
The Issue: There is over-molding that stabilizes the connection between the cable and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...
The Issue: There is over-molding that stabilizes the connection between the cable and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...
The Issue: Potential for certain SKUs and lot numbers were distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Recalled...
The Issue: Potential for certain SKUs and lot numbers were distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...
The Issue: Potential for certain SKUs and lot numbers were distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) MTO Recalled by MEDLINE...
The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) FDS Recalled by MEDLINE...
The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LithoCrushV Single Use Mechanical Lithotriptor V. Model Number:...
The Issue: Potential for distal tip tearing of the Mechanical Lithotriptor V.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1)...
The Issue: Complaints have been received regarding post-operative implant collapse.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Premium Dressing Change Kit with Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: IMed Products Product Name: Dressing Change Kit with Recalled by...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Transparent...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.