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. 2,652 recalls have been distributed to Kentucky in the last 12 months.
Showing 4921–4940 of 13,398 recalls
Recalled Item: Estriol Recalled by Medisca, Inc. Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VCF Vaginal Contraceptive Foam Recalled by Apothecus Pharmaceutical Corp....
The Issue: Defective Delivery System: canister unit exhibiting propellant leakage or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Petroleum jelly (White Petrolatum) USP 100% Recalled by OraLabs,...
The Issue: Cross contamination with other products: undeclared contaminants of phenol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EXPAREL Recalled by Pacira Pharmaceuticals, Inc. Due to Sub Potent Drug: Out...
The Issue: Sub Potent Drug: Out of Specification (OOS)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant &...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by AuroMedics Pharma LLC Due to Presence of...
The Issue: Presence of Foreign Tablets/Capsules: One Losartan/HCTZ tablet was found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags Recalled by Baxter...
The Issue: Lack of Assurance of Sterility: Product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...
The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colostat Recalled by Grato Holdings, Inc. Due to Labeling mix-up -...
The Issue: Labeling mix-up - Indications on product label are incorrect.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.