Recalls / Class II
Class IID-0528-2024
Product
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Roll-On 3 fl oz (88.7ml), painwizard.com Made in the USA, PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00010 9
- Affected lot / code info
- Lot 17323C3, Exp 06/30/2025
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
- 3,504
- 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-0528-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.