D-0528-2024 Class II Ongoing
FDA drug recall D-0528-2024 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: 3,504.
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
- 3,504
Product Description
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
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
Lot 17323C3, Exp 06/30/2025