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. 2,609 recalls have been distributed to Kentucky in the last 12 months.
Showing 10921–10940 of 28,748 recalls
Recalled Item: VITROS Chemistry Products Performance Verifier II-For in vitro diagnostic...
The Issue: Product instability; biased ALKP values obtained from VITROS Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) Ventilator Series - Product Usage: for Recalled...
The Issue: In-house lab observations and customer reports of overheating and/or thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Zyphr Disposable Cranial Perforator Recalled by Stryker Instruments...
The Issue: Potential for the inner bit to contain a crack, that may or may not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous...
The Issue: 5F Micro-Introducer Kits may not contain the correct device, packaged with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...
The Issue: Luminex has determined that three (3) separate test fixtures used by field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...
The Issue: Luminex has determined that three (3) separate test fixtures used by field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard - Product Usage: Obstetric Gynecologic specialized manual instrument....
The Issue: Labeling error, incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminesse ML PMMA Recalled by Talladium Inc Due to Heat-cured...
The Issue: Heat-cured polymethylmethacrylate (PMMA) milling blank product used to make...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas infinity central lab/cobas infinity core license-The cobas infinity IT...
The Issue: Potential Incorrect Validation of Results Due to an Erroneous QC Status When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InSure ONE Test Strips (25 pack) vials-fecal immunochemical test (FIT)...
The Issue: Product does not meet internal testing criterion; use of the product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Recalled by...
The Issue: There is a potential that the cable of the Flat panel detector may break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation standalone software treatment planning system Recalled by...
The Issue: If a region of interest (ROI) or point of interest (POI) that is from an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog 02145P Recalled by Microbiologics Inc Due to Strain should be VIM-1...
The Issue: Strain should be VIM-1 positive but is confirmed to be VIM-1 negative.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Leak Test Adapter used with Acu-sInQ Complete Endoscope Cleaning...
The Issue: Potential for cleaning solution intrusion into endoscope
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used Recalled by...
The Issue: Risk of Sling Clip breakage while in use with obsolete Flat Dynamic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog 314-13-23 Recalled by Exactech, Inc. Due to Mislabeling
The Issue: The product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.