Product was from unapproved source.
All Recalls
95,018 total recalls in our database
Due to presence of mold on product
Product was from unapproved source.
Product was from unapproved source.
Fish is declared but specific fish name is not declared on Fish-pickle.
Product was from unapproved source.
Product was from unapproved source.
Failed Dissolution Specifications
Defective Container: The notch in the cap that fits into the nozzle of the dropper could break off and block the dropper possibly resulting in the product not dispensing.
Failed Dissolution Specifications
Labeling: Missing Label: label missing from some Semglee prefilled pens.
Failed Dissolution Specifications
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Failed Dissolution Specifications
Failed Dissolution Specifications
Failed Dissolution Specifications
Clobetasol Propionate Foam, 0.05%, packaged in a) 50 g can (NDC 50742-304-50), and b) 100 g can (NDC 50742-304-01), Rx only, Manufactured for: Ingenus Pharmaceuticals, LLC, Orlando, FL 32839-6408.
Ingenus Pharmaceuticals
CGMP Deviations
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3
Dr. Reddy's Laboratories
Subpotent drug
Failed Dissolution Specifications