Soltice Quick-RUB
CGMP DEVIATIONS
Yes — there is an active recall. 20 ongoing FDA recalls mention Camphor (34 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Camphor. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
CGMP DEVIATIONS
CGMP DEVIATIONS
CGMP DEVIATIONS
CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.
CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.
CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.
CGMP Deviations: products were manufactured with lack of process validation, cleaning validation, stability studies, and other current good manufacturing practice violations.
Superpotent Drug: high out of specification assay results for the camphor ingredient.
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