Recalls / Class II
Class IID-0525-2024
Product
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
- Affected lot / code info
- Lot , 06023C1, 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
- 2,864
- 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-0525-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.