US Drug Recall Register

FDA Drug Recalls

14,450 recalls · Class II, newest first

Class II · Moderate risk Terminated

Regular Strength Pain Reliever

Reason cGMP deviations

Ultra Seal Corporation NDC 67060-0113-00 D-0498-2022
Class II · Moderate risk Terminated

Mint Flavored Antacid

Reason cGMP deviations

Ultra Seal Corporation NDC 67060-303-68 D-0496-2022
Class II · Moderate risk Terminated

PAINAID PMF Premenstrual Formula

Reason cGMP deviations

Ultra Seal Corporation NDC 42961-0046-03 D-0494-2022
Class II · Moderate risk Terminated

PAINAID BRF Back Relief Formula

Reason cGMP deviations

Ultra Seal Corporation NDC 42961-0003-00 D-0493-2022
Class II · Moderate risk Terminated

Painaid

Reason cGMP deviations

Ultra Seal Corporation D-0492-2022
Class II · Moderate risk Terminated

Extra Strength Un-Aspirin

Reason cGMP deviations

Ultra Seal Corporation NDC 42961-041-03 D-0491-2022
Class II · Moderate risk Terminated

Dilotab II

Reason cGMP deviations

Ultra Seal Corporation NDC 42961-052-03 D-0490-2022
Class II · Moderate risk Terminated

Cold Relief

Reason cGMP deviations

Ultra Seal Corporation NDC 42961-112-03 D-0483-2022
Class II · Moderate risk Terminated

Backache & Muscle Relief

Reason cGMP deviations

Ultra Seal Corporation NDC 42961-111-83 D-0482-2022
Class II · Moderate risk Terminated

Multi-Symptom Cramp Relief

Reason cGMP deviations

Ultra Seal Corporation D-0481-2022
Class II · Moderate risk Terminated

Multi Symptom Cold Relief

Reason cGMP deviations

Ultra Seal Corporation D-0478-2022
Class II · Moderate risk Terminated

Back Pain-Off

Reason cGMP deviations

Ultra Seal Corporation NDC 47682-073-00 D-0476-2022
Class II · Moderate risk Terminated

MidNite Sleep Health

Reason cGMP deviations

Ultra Seal Corporation D-0475-2022
Class II · Moderate risk Terminated

Dologen

Reason cGMP deviations

Ultra Seal Corporation NDC 52083-482-02 D-0474-2022