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. 2,474 recalls have been distributed to Kentucky in the last 12 months.
Showing 21901–21920 of 28,748 recalls
Recalled Item: Prism Medical P-300 Portable Consumer Lift Recalled by ErgoSafe Products,...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis...
The Issue: Complaints that the femoral head could not be assembled with its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical C-300 Consumer Ceiling Lift Recalled by ErgoSafe Products, LLC...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialist 2 Intramedullary (SP2 IM) Rod 400mm Instrument (PN 96-6120)...
The Issue: DePuy Orthopaedics, Inc. is initiating a voluntary recall of select lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Pipeline Embolization Device -Pipeline Flex Embolization Device The...
The Issue: The firm is recalling Pipeline and Pipeline Flex Embolization Devices from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnVision FLEX/HRP visualization reagent found in the following kits:...
The Issue: There is a defect in one lot of a buffer, non-specific background staining...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.0mm Unit Rod 270mm Recalled by Synthes (USA) Products LLC Due to This...
The Issue: This product was produced using a finishing process not identified as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inserter for Titanium Elastic Nails (TEN) Recalled by Synthes (USA) Products...
The Issue: potential for mechanical failures such as breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 400 and AMSCO C Small Steam Sterilizers Recalled by Steris Corporation...
The Issue: In AMSCO Small Steam Sterilizers equipped with the CS-iQ feature, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer...
The Issue: In about 5% of tested samples, the outer tray was found to be compromised....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 123 POC system The cobas b 123 POC Recalled by Roche Diagnostics...
The Issue: under specific settings, an issue may occur during simultaneous Sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10)....
The Issue: These Lot numbers are not stable up to the expiry date on the product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A) Recalled by Bausch & Lomb...
The Issue: The firm determined that 25 lots had been manufactured with a minor surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CryoConsole Recalled by Medtronic Inc. Cardiac Rhythm Disease...
The Issue: An issue with a USB memory component contained within a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Recalled by AGFA Healthcare Corp. Due to Customers have experienced...
The Issue: Customers have experienced IMPAX CV software, specifically, Demographics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.