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. 983 recalls have been distributed to Kentucky in the last 12 months.
Showing 36821–36840 of 51,386 recalls
Recalled Item: Software version VD10E for Syngo X-Workplace Recalled by Siemens Medical...
The Issue: Potential post-processing software issue when using tabcard "4D" on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...
The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCM CombiM Modules 903-111 Recalled by Radiometer America Inc Due to...
The Issue: Radiometer America, Inc. is recalling TCM CombiM on rare occasions they may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressit-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...
The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Recalled by...
The Issue: Lumenis Ltd Announces a Field Action of the M22 IPL Acne Filters for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...
The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...
The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...
The Issue: Some tubes were manufactured with the stopper not fully inserted into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer frozen Butternut Squash Ravioli Recalled by Bertagni 1882 Due to...
The Issue: Meijer frozen Butternut Squash Ravioli is recalled because product may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bertagni fresh Sweet Butternut Squash Ravioli Recalled by Bertagni 1882 Due...
The Issue: Bertagni fresh Sweet Butternut Squash Ravioli is recalled because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BAKERY FRESH GOODNESS Chocolate Brownie NET WT 16 OZ (1 LB) 453 g CONTAINS:...
The Issue: The firm was notified by a consumer of undeclared walnuts in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: iCup DX 8 Panel w/Adulterant Recalled by Ameditech Inc Due to Ameditechs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS Diagnostic Viewer versions 8.3.7 Recalled by Novarad Corporation...
The Issue: The SUV values that are being calculated in the PET/CT fusion tool are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen 6 Panel Cassette w/Adult (AU) Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDI BZO Uncut Sheet - Cup* Recalled by Ameditech Inc Due to Ameditechs Drugs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.