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. 2,634 recalls have been distributed to Kentucky in the last 12 months.
Showing 8241–8260 of 28,748 recalls
Recalled Item: Sara Plus Active Floor Lift Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o. Due...
The Issue: The device may emit smoke or ignite.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Heater within...
The Issue: Heater within the Verigene System may be outside of established temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The following first aid kits and cabinets containing components Medi-First...
The Issue: First aid kit and cabinet components are being recalled by the supplier due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Kit SARS-cCo V Antigen Rapid Test Recalled by USA Medical, LLC...
The Issue: COVID-19/SARS-CoV-2 Antigen Tests did not receive FDA Emergency Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272V CMOS VIDEO-CYSTO-URETHROSCOPE REV 11272VA 11272VAK CMOS...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 9100-Series Washer Disinfector models: 9120E Recalled by Getinge Usa...
The Issue: Inadequate documentation verifying whether device installation has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278A2 11278AK2 Flexible Ureteroscope Z20615US-BA (08-2018) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CYSTO-URETHRO-FIBERSCOPE CYSTOSCOPE Recalled by Karl Storz Endoscopy Due to...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VH-TL 11272VHK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11274BCU1 11274BCUK1 Flexible Cystoscope Z18449US-BD (08-2018) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VUE 11272VUEK Flexible Video Cysto-Urethroscope 96136031USCA V1.1...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278V 11278VK CMOS Video Ureteroscope Z17744US-A (04/2016) Recalled by Karl...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flo-Thru Intraluminal Shunt. Used in coronary artery or peripheral vascular...
The Issue: There is a potential for foreign matter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Celltrion DiaTrust COVID-19 Ag Rapid Test Recalled by CELLTRION USA INC Due...
The Issue: Point of Care (PoC) rapid test products were distributed to customers who...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 Fr -For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.