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. 2,609 recalls have been distributed to Kentucky in the last 12 months.
Showing 12801–12820 of 13,398 recalls
Recalled Item: Magnesium Sulfate 2 grams in Dextrose 5% for Injection Recalled by Med Prep...
The Issue: Non-Sterility; mold contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jolessa (levonorgestrel/ethinyl estradiol) Tablets Recalled by Teva...
The Issue: Failed Tablet/Capsule Specifications: This recall is being carried out due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by L. Perrigo Co. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: 3 month stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Portia (levonorgestrel and ethinyl estradiol) Tablets Recalled by Teva...
The Issue: Failed Tablet/Capsule Specifications: This recall is being carried out due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Night Bullet Capsules Recalled by Green Planet Inc Due to Marketed Without...
The Issue: Marketed Without an Approved NDA/ANDA; product contains analogues of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLETS Recalled by Gsms Due to Presence...
The Issue: Presence of Foreign Substance: Reports of gray smudges identified as minute...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetic Acid Otic Solution Recalled by Hi-Tech Pharmacal Co., Inc. Due to...
The Issue: Subpotent Drug: The product/lot is out-of-specification (OOS) for the assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Nasal Decongestant Fast Acting Nasal Spray Recalled by Novartis...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Myoflex (trolamine salicylate) 10% Recalled by Novartis Consumer Health Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nupercainal Recalled by Novartis Consumer Health Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Nasal Decongestant Menthol Nasal Spray Recalled by Novartis Consumer...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifadin Recalled by Sanofi US Due to Subpotent drug: low fill volume in some...
The Issue: Subpotent drug: low fill volume in some of the capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Saline Moisturizing Mist with Eucalyptol & Menthol Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol Recalled by CareFusion...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v Recalled by CareFusion 213,...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol) Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 10% Povidone Iodine Solution USP (1% available Iodine Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.