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. 2,628 recalls have been distributed to Kentucky in the last 12 months.
Showing 10481–10500 of 13,398 recalls
Recalled Item: Rose Bengal GloStrips (rose bengal) Ophthalmic Strips USP Recalled by Nomax...
The Issue: Failed Content Uniformity Specifications: The product may not meet finished...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...
The Issue: Failed Content Uniformity Specifications: The product may not meet finished...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...
The Issue: Failed Content Uniformity Specifications: The product may not meet finished...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clinimix E 5/20 sulfite-free (5% amino-acid with electrolytes in 20%...
The Issue: Lack of Assurance of Sterility; increased complaints received for leaks
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp Due to...
The Issue: Lack of Assurance of Sterility; increased complaints received for leaks
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Injection Recalled by Mylan Institutional LLC Due to Presence...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CARBOplatin Injection 450 mg/45 mL (10 mg/mL) Recalled by Mylan...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captopril Tablets Recalled by Wockhardt Usa Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: out of specification for thickness.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACTATED RINGER'S IRRIGATION Recalled by Hospira Inc. Due to Non-Sterility:...
The Issue: Non-Sterility: Confirmed customer report of dark, fibrous particulates...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine HCl Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 83/17 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRIOL (E3) W/V (weight/volume) PGF 0.1% (1.0MG/ML) Transdermal cream...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.