US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Mar 10, 2021 (5 years ago)

aulief (Organic Camphor 3.00% Organic Menthol 5.00%), topical pain relief, packaged as a)…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.

What was recalled

aulief (Organic Camphor 3.00% Organic Menthol 5.00%), topical pain relief, packaged as a) 3.2 oz (90.7g) tube UPC 6 87806 30003 1 NDC 76305-302-01 ; b) 7.0 oz (198.5g) tube, UPC 6 87806 30007 9, NDC 76305-302-02; c) 16 oz (453.6g)Bottle w/ Pump, UPC 6 87806 30016 1, NDC 76305-302-03; Distributed by: CHINA-GEL LLC, Arlington Heights, IL 60005,

Recalling firm
China Gel Inc
NDC code
76305-302-01
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0790-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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