D-0524-2024 Class II Ongoing
FDA drug recall D-0524-2024 was initiated by ARG Laboratories, Inc. on April 17, 2024 and is designated Class II. Reason for recall: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process. The recall status is ongoing. Affected quantity: 7,410.
Recall Details
- Product Type
- Drugs
- Report Date
- June 5, 2024
- Initiation Date
- April 17, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7,410
Product Description
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
Reason for Recall
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Distribution Pattern
Distributed Nationwide in the USA
Code Information
Lots 19823C4, EXP 07/31/2025; 01623C1, Exp 01/31/2025