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. 2,625 recalls have been distributed to Kentucky in the last 12 months.
Showing 12101–12120 of 13,398 recalls
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bethel 30 capsules Recalled by Bethel Nutritional Consulting, Inc Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VECURONIUM Bromide for Injection Recalled by Sagent Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: product was not manufactured under current good...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Excedrin Migraine (Acetaminophen 250 mg Recalled by Novartis Consumer Health...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Parsel Plus ( US product: Excedrin Tension Headache) (Acetaminophen 500...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Excedrin Extra Strength (Acetaminophen 250 mg Recalled by Novartis Consumer...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The product has the potential for solution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: No Doz Recalled by Novartis Consumer Health Due to Defective container:...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cleocin Phosphate (clindamycin Injection) Recalled by Pharmacia & Upjohn LLC...
The Issue: Presence of Particulate Matter: Firm is recalling a small number of vials...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625...
The Issue: Failed Dissolution Specifications: Pfizer Inc. (Pfizer) is recalling PREMPRO...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norpace CR (disopyramide phosphate) extended-release capsules USP Recalled...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625...
The Issue: Failed Dissolution Specifications: Pfizer Inc. is recalling PREMPRO...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefazolin Recalled by Sandoz Incorporated Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Sandoz Inc is recalling Cefazolin for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pharmalucence Kit for the Preparation of Technetium Tc 99m Sestamibi...
The Issue: Presence of Particulate Matter; particulate found in retain samples
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Detomidine 10 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beta Alanine 100 mg/ml / l-carnosine 100 mg/ml Injection Recalled by Lowlite...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.