Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Is Zinc recalled?

Yes — there is an active recall. 47 ongoing FDA recalls mention Zinc (156 total). Check the affected lots below.

Recalls are matched by product description. A recall usually affects specific lots, not every package of Zinc. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.

Zinc recalls on record

none so far in 2026; 156 on record, newest first
Class II · Moderate risk

Renew PeriProtect

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Ongoing cGMP deviation DermaRite Industries, LLC NDC 61924-435-04 D-0174-2026
Class II · Moderate risk

Ultra Violette

Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.

Ongoing Wrong potency / content Grace & Fire Pty LTD NDC 84803-106-01 D-0640-2025
Class II · Moderate risk

Rapidol

CGMP Deviations

Terminated cGMP deviation Kenil Healthcare Private Limited NDC 55758-440-02 D-0429-2025
Class III · Low risk

Badger 50

Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use.

Terminated Labeling / mix-up The W.S. Badger Company, Inc. D-0209-2025
Class II · Moderate risk

babyganics

Failed stability specifications: during routine stability monitoring quality concerns were identified. Physical separation for ingredients was observed.

Ongoing Stability / shelf life Johnson, S C and Son, Inc D-0298-2025
Class II · Moderate risk

suntegrity

CGMP Deviations

Ongoing cGMP deviation Synchronicity Spa INC, Dba Sunte D-0589-2024
Class I · High risk

suntegrity

Microbial Contamination of Non-Sterile Products: Presence of Aspergillus Sydowii (Mold)

Ongoing Microbial contamination Synchronicity Spa INC, Dba Sunte D-0588-2024
Class II · Moderate risk

Unguentine Ointment

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Completed cGMP deviation Ecometics, Inc. D-1099-2023
Class II · Moderate risk

Ak-Poly-Bac

CGMP Deviations: Firm went out of business and could no longer continue stability studies.

Ongoing Stability / shelf life Akorn, Inc. D-0788-2023
Class II · Moderate risk

Triple Antibiotic Ointment

CGMP Deviations: products were stored outside the drug label specifications.

Terminated Labeling / mix-up Mckesson Medical-Surgical Inc. Corporate Office NDC 0498-0750-36 D-1311-2022