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 9981–10000 of 51,386 recalls
Recalled Item: MEKTOVI (binimetinib) tablets Recalled by Pfizer Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AQURE Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 Recalled by Radiometer...
The Issue: Due to potential software issue that may result in patient mix-up information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems Recalled by...
The Issue: Due to manufacturing issue, Gastrointestinal (GI) Panel may result in false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray...
The Issue: Issue related to the operation of the arm latch within the column that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr. Rima Recommends The Silver Solution Immune System Support Dietary...
The Issue: Product labeled and intended to mitigate, prevent, or treat COVID-19
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual....
The Issue: Error in the Introduction section of the user manual that indicates the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Recalled by Maquet Cardiovascular, LLC Due to Some batches...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 R1.1 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcitonin Salmon Nasal Spray Recalled by Endo Pharmaceuticals, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications and Subpotent Drug: High Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobazam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.