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. 2,630 recalls have been distributed to Kentucky in the last 12 months.
Showing 9901–9920 of 28,748 recalls
Recalled Item: ELI 380 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mark 910 LogiCal Recalled by Smiths Medical ASD Inc. Due to Specific lots of...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...
The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Recalled by Nobel Biocare...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Provox Life Night HME Recalled by Atos Medical AB Due to Provox Life Night...
The Issue: Provox Life Night HME may be incorrectly inserted sideways or forcefully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for Recalled by...
The Issue: 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75...
The Issue: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Xper Flex Cardio (FC2010 Recalled by Philips North America Llc Due...
The Issue: Performance issues with the Xper Flex Cardio Physio Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...
The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Dressing Change Tray Recalled by ROi CPS LLC Due to ChloraPrep...
The Issue: ChloraPrep applicators in the kit can grow organisms that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...
The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InCore Lapidus Disposable Kit 28mm Left Recalled by Nextremity Solutions Due...
The Issue: Product could potentially contain an undersized inner diameter of the 40mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number:...
The Issue: Some Artis zee ceiling systems show an increased abrasion of the cabling at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InCore Lapidus Disposable Kit 28mm Right Recalled by Nextremity Solutions...
The Issue: Product could potentially contain an undersized inner diameter of the 40mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.