Recalling firm
ARG Laboratories, Inc.
Product type
Drug
Status
Ongoing
Report date
2024-06-05
Distribution
Distributed Nationwide in the USA
Firm state
TX
Product quantity
2,864
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & QualificationReason for recall
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Product description
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube, NET WT 4oz (113.39g), painwizard.com Made in the USA, PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00019 2
Code / lot info
Lot , 06023C1, Exp 01/31/2025,
Other recalls SPEQ maps to Validation & Qualification
See all Validation & Qualification recalls →Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.