HTO Nevada Inc. Recalls Lidocaine Cream Due to Stability Data

HTO Nevada Inc. is recalling its MAXIMUM, ZONE 1, 4% Lidocaine Cream (NDC 80069-014) nationwide due to stability data not supporting the expiry date. This is a Class II recall, indicating that use of or exposure to the product may cause temporary or medically reversible adverse health consequences.

ACME UNITED CORPORATION Class II Drug Recall D-0358-2026

The FDA has initiated a Class II drug recall (D-0358-2026) for ACME UNITED CORPORATION's First Aid Only BZK Antiseptic Towelettes due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects a nationwide distribution within the United States.

ACME UNITED CORPORATION Class II Drug Recall D-0369-2026

The FDA has initiated a Class II drug recall (D-0369-2026) for Dynarex Obstetrical Towelettes Cleanser manufactured by ACME UNITED CORPORATION due to CGMP deviations. The recall affects product distributed nationwide within the United States.

New Life Pharma LLC Class II Drug Recall for Tirzepatide Inj

The FDA has initiated a Class II drug recall for New Life Pharma LLC's Tirzepatide Inj (NDC 84223-002-03) due to a lack of assurance of sterility. The recall affects product distributed in Ohio.

New Life Pharma LLC Class II Drug Recall - Semaglutide Inj

The FDA has issued a Class II drug recall for Semaglutide Inj manufactured by New Life Pharma LLC due to a lack of assurance of sterility. The recall affects product distributed in Ohio.

ACME UNITED CORPORATION Class II Drug Recall D-0375-2026

The FDA has initiated a Class II drug recall for ACME UNITED CORPORATION's Dynarex BZK Antiseptic Towelettes due to CGMP deviations. The recall affects product distributed nationwide in the United States.

Teva Pharmaceuticals Class II Recall: Metoprolol Succinate Tablets

The FDA has initiated a Class II recall for Teva Pharmaceuticals' Metoprolol Succinate Extended-Release Tablets due to failed dissolution specifications. The recall affects nationwide distribution and is ongoing.

ACME UNITED CORPORATION Class II Recall for Alcohol Hand Wipe

The FDA has initiated a Class II recall for ACME UNITED CORPORATION's Antimicrobial Alcohol Hand Wipe due to CGMP deviations. The recall affects product distributed nationwide in the United States and is currently ongoing.

ACME UNITED CORPORATION Class II Drug Recall

The FDA has initiated a Class II drug recall for ACME UNITED CORPORATION's Max Packaging Antibacterial Towelette due to CGMP deviations. The recall affects product distributed nationwide within the United States and is ongoing.

ACME UNITED CORPORATION Class II Recall of Antiseptic Wipes

The FDA has announced a Class II recall for ACME UNITED CORPORATION's Medi-First Antiseptic Wipes due to CGMP deviations. The recall affects product distributed nationwide in the United States.