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. 2,509 recalls have been distributed to Kentucky in the last 12 months.
Showing 17981–18000 of 28,748 recalls
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....
The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....
The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal(R) Dolphin Inflation Device Recalled by DeRoyal Industries Inc Due...
The Issue: Lack of sterility assurance. There is a defect in the primary packaging of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....
The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid...
The Issue: Potential for flouroscopially visible marker band at the tip of the Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis Recalled by Siemens Medical Solutions USA, Inc Due to Potential...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.Zen Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.