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Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Yes — there is an active recall. 51 ongoing FDA recalls mention Menthol (132 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Menthol. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
CGMP Deviations: Potential Glass and Silicone particulates in product
CGMP Deviations: Potential Glass and Silicone particulates in product
CGMP Deviations: Potential Glass and Silicone particulates in product
CGMP Deviations: Potential Glass and Silicone particulates in product
CGMP Deviations: Potential Glass and Silicone particulates in product
Incorrect/Undeclared Excipients.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP DEVIATIONS
CGMP DEVIATIONS
CGMP DEVIATIONS
Superpotent Drug: product complaint for milky blue appearance and consistency, further investigation by the firm found the recalled lots out of specification for the four active ingredients.
Subpotent drug: Low OOS for menthol content at the three month room temperature.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
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