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

Yes — there is an active recall. 1 ongoing FDA recall mention Arnica (16 total). Check the affected lots below.

Most common reason: Microbial contamination (8 of these recalls)

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

Arnica recalls on record

none so far in 2026; 16 on record, newest first
Class II · Moderate risk

ZTE-1035 Formula

Out-of-specification test results obtained for identification testing based on HPTLC analysis.

Terminated Failed specification Washington Homeopathic Products, Inc. D-0886-2021
Class II · Moderate risk

Workvie Instant Pain Relieving Roll On

CGMP Deviations: products were manufactured with lack of process validation, cleaning validation, stability studies, and other current good manufacturing practice violations.

Terminated Stability / shelf life Pharma-Natural Inc. NDC 72393-201-25 D-1507-2019
Class II · Moderate risk

Arnica Power

CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.

Terminated Microbial contamination Sprayology NDC 61096-0032-1 D-0117-2019