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. 2,646 recalls have been distributed to Kentucky in the last 12 months.
Showing 5481–5500 of 28,748 recalls
Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...
The Issue: Elevated results were detected with Li-heparin plasma samples when compared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edge Biologicals STERILE WATER Recalled by Edge Biologicals Inc Due to Due...
The Issue: Due to product outer packaging incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...
The Issue: Unexpected failure of electrical components within the CPI generator.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT-Site M BHB Test Strips Recalled by Stanbio Laboratory, LP Due to...
The Issue: Deterioration in the stability of the Test Strips results in diminished...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation...
The Issue: Sterilization failures when devices are sterilized per the Reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray Recalled...
The Issue: There is a potential for unexpected failure of the electrical components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coapt Dome Electrode Recalled by Coapt LLC Due to Patient may experience...
The Issue: Patient may experience minor burn or blistering if device is exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coapt ControlSeal Electrode Recalled by Coapt LLC Due to Patient may...
The Issue: Patient may experience minor burn or blistering if device is exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO +VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO VISIAN Implantable Collamer Lens .2. Phakic Intraocular lens. Recalled...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.