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. 979 recalls have been distributed to Kentucky in the last 12 months.
Showing 37801–37820 of 51,386 recalls
Recalled Item: LIDocaine HCl 1% BUFFERED WITH SODIUM BICARBONATE Injection Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Midazolam HCl in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL citrate in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL CITRATE 4 MCG/mL in 0.9% SODIUM CHLORIDE Injection Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN Sodium in 0.45% Sodium Chloride Recalled by Cantrell Drug Company...
The Issue: Stability Data Does Not Support Expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIDAZOLAM HCl in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn, Inc. Due to...
The Issue: Defective Container: Product missing safety seal around the neck of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL citrate in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL Citrate 50 mcg/mL in Sterile Water for Injection Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution...
The Issue: Lack of Assurance of Sterility; potential exposure to non-sterile lubricant...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamivudine Oral Solution Recalled by Silarx Pharmaceutical, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator...
The Issue: Discoloration
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL CITRATE 25 mcg/mL in 5% DEXTROSE Injection Recalled by Cantrell...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIDAZolam HCl 0.1 mg/mL in 5% DEXTROSE 2.5 mL syringe Recalled by Cantrell...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL Citrate 1 MCG/mL in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RIFAMPIN FOR INJECTION USP Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurity/Degradation Specifications: Out of Specifications result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketamine Hydrochloride Injection Recalled by Hospira Inc. Due to Defective...
The Issue: Defective Container: There were customer complaints of cracked and leaking...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aliquot Delivery Kit (Syringe and Plunger) Recalled by Orthovita, Inc., dBA...
The Issue: Two isolated instances of holes in the outer header bag component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Deep All Natural Spices Coriander Powder Recalled by Chetak New York, LLC...
The Issue: Chetak New York L.L.C. of Edison, NJ is recalling 300 jars of 14.1oz Deep...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.