← FDA ENFORCEMENT
D-0520-2024Class II

ARG Laboratories, Inc.

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
3,440
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & Qualification
Reason 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, Bottle with pump, NET WT 16 fluid oz / 473.17 ml, Made in USA, www.painwizard.com Pain Wizard LLC.PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00012 3

Code / lot info

Lot: 18723C3, Exp 06/30/2025

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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.