US Drug Recall Register

FDA Drug Recalls

11,815 recalls · Class II, newest first

Class II · Moderate risk Terminated

Syphilinum

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1138-2022
Class II · Moderate risk Terminated

Streptococcinum

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1137-2022
Class II · Moderate risk Terminated

Pyrogenium

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1136-2022
Class II · Moderate risk Terminated

Proteus

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1135-2022
Class II · Moderate risk Terminated

Pertussinum

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1134-2022
Class II · Moderate risk Terminated

Morbillinum

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1133-2022
Class II · Moderate risk Terminated

Medorrhinum

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1132-2022
Class II · Moderate risk Terminated

Influenzinum

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1131-2022
Class II · Moderate risk Terminated

Diphtherinum

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1130-2022
Class II · Moderate risk Terminated

Colibacillinum

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1129-2022
Class II · Moderate risk Terminated

Candida Parapsilosis

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1128-2022
Class II · Moderate risk Terminated

Candida Albicans

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1127-2022
Class II · Moderate risk Terminated

Bacillinum Pulmo

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1126-2022
Class II · Moderate risk Terminated

Anthracinum

Reason cGMP deviations

Washington Homeopathic Products, Inc. D-1125-2022
Class II · Moderate risk Terminated

Zonisamide Capsules USP

Reason CGMP Deviations: Gaps in the quality system in the Quality Control microbiology laboratory.

Direct Rx NDC 61919-775-90 D-0888-2022
Class II · Moderate risk Terminated

Equate Tartar Control Plus

Reason Superpotent Drug: product complaint for milky blue appearance and consistency, further investigation by the firm found the recalled lots out of specification for the four active ingredients.

Vi-Jon, LLC D-0970-2022