Mutual Pharmaceutical Company Sulfamethoxazole and Trimethoprim Tablets, USP, 800 mg/160 mg recall — FDA D-0572-2016
Presence of foreign substance -This recall has been intiated due to the presence of a polyethylene piece on the finished product.
Overview of recall records associated with Mutual Pharmaceutical Company, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 4.
Presence of foreign substance -This recall has been intiated due to the presence of a polyethylene piece on the finished product.
cGMP Deviations; Clonidine hydrochloride drug substance used in the manufacturing of this product, was dispensed in unauthorized rooms by the drug substance manufacturer
cGMP Deviations; Clonidine hydrochloride drug substance used in the manufacturing of this product, was dispensed in unauthorized rooms by the drug substance manufacturer
cGMP Deviations; Clonidine hydrochloride drug substance used in the manufacturing of this product, was dispensed in unauthorized rooms by the drug substance manufacturer
This page summarizes recall records in which the official source identifies Mutual Pharmaceutical Company, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.