AAA Pharmaceutical, Inc. Recalls

FDA
4
Total Recalls
1
Agencies
Aug 2019
First Recall
Mar 2020
Latest Recall

Showing 1-4 of 4 recalls

FDA

Discount Drug Mart, Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg /Antihistamine, Indoor/Outdoor Allergies, 24 Hour, a) 30 tablets per bottle, NDC 53943-192-04, UPC Code 0-93351-03069-7; b) 45 tablets per bottle, NDC 53943-192-06, UPC Code 0-93351-03070-3, Distributed by: Drug Mart -Food Fair, 211 Commerce Drive, Medina, OH 44256.

Labeling: Incorrect or Missing Lot and/or Expiration date.

FDA

Ranitidine 150 mg tablets, 130 count bottles, NDC 37808-196-04.

CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

FDA

Ranitidine 150 mg tablets, 24 count bottles, NDC 37808-196-01.

CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

FDA

Smart Sense Regular Strength Aspirin Tablets, 325 mg packed in a) 100 count UPC 8-8397-38781-6 and b) 500 count UPC 8-83967-38786-1 bottles, Distributed by: Kmart Corporation Hoffman Estates, IL 60179

Labeling; Incorrect or Missing Lot Number and/or Exp Date; Product has an incorrect expiration date of 9/2022 applied to the labeling, where the actual expiration date is 10/2021.