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. 1,726 recalls have been distributed to Kentucky in the last 12 months.
Showing 47941–47960 of 51,386 recalls
Recalled Item: Lidocaine Injection Recalled by FVS Holdings, Inc. dba. Green Valley Drugs...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin D3 Injection Recalled by FVS Holdings, Inc. dba. Green Valley Drugs...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Procaine Hydrochloride Injection Recalled by FVS Holdings, Inc. dba. Green...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets Recalled by Aurobindo Pharma USA Inc Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength: Incorrect strength on side...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medi-First Brand First Aid Kit Recalled by Total Resources Intl Due to CGMP...
The Issue: CGMP Deviations: The first aid kits that are subject to the voluntary recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3M Tekk Brand Industrial/Construction First Aid Kit Recalled by Total...
The Issue: CGMP Deviations: The first aid kits that are subject to the voluntary recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: (No Brand) First Aid Kit Recalled by Total Resources Intl Due to CGMP...
The Issue: CGMP Deviations: The first aid kits that are subject to the voluntary recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natus neurology Dantec KEYPOINT.NET 2.20. Catalog/Part Numbers: 9031A070103...
The Issue: Alpine Biomed ApS is recalling Natus neurology Dantec KEYPOINT.NET ver. 2.20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL RecombiPlasTin 2G Recalled by Instrumentation Laboratory Co. Due to...
The Issue: Instrumentation Laboratory is recalling HemosIL RecombiPlasTin 2G (RPT2G),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermalight 80 Model Number UVB-080 Recalled by National Biological Corp Due...
The Issue: The incorrect manual may have been packaged with this product. UVB-080...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an...
The Issue: Several complaints were recorded regarding one of the three screws driving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defribillator Recalled by Philips Healthcare Inc. Due...
The Issue: Device may fail to deliver defibrillation therapy in either Manual Defib or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endopath Electrosurgery Probe Plus II Recalled by Ethicon Endo-Surgery Inc...
The Issue: The firm is recalling the ENDOPATH Probe Plus II Shafts because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: A single visible particulate was identified...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.