Recalls / Class II
Class IID-0524-2024
Product
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube, NET WT 8 oz (226.79g), Made in the USA, painwizard.com PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00011 6
- Affected lot / code info
- Lots 19823C4, EXP 07/31/2025; 01623C1, Exp 01/31/2025
Why it was recalled
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Recalling firm
- Firm
- ARG Laboratories, Inc.
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 2639 Manana Dr, Dallas, Texas 75220-1301
Distribution
- Quantity
- 7,410
- Distribution pattern
- Distributed Nationwide in the USA
Timeline
- Recall initiated
- 2024-04-17
- FDA classified
- 2024-05-30
- Posted by FDA
- 2024-06-05
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0524-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.