Severity
Moderate
ModerateClass IIOngoing
FDA Drug recall · Reported June 5, 2024
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Bottle with pump, NET WT 16 fluid oz / 473.17 ml, Made in USA, www.painwizard.com Pain Wizard LLC.PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00012 3
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Arg Laboratories, Inc. recalled Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enr… - a moderate-severity action.
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enr… was recalled by Arg Laboratories, Inc. in June 5, 2024. Reason: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing…. Check the official notice for the remedy. Verify recall #D-0520-2024 with the FDA Drug before acting.
The recall
Arg Laboratories, Inc. issued this moderate-severity FDA Drug recall-Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing….
- Moderate
- severity level
- 3K units
- affected scope
- Class II
- classification
- June 5, 2024
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0520-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0520-2024) was formally reported on June 5, 2024, with the manufacturer initiating the action on April 17, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. Arg Laboratories, Inc. is listed as the recalling firm, operating out of Dallas, TX. Federal records list the affected scope as 3,440.
The documented reason for this recall is: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process. Distribution data in the federal record shows the product reached: Distributed Nationwide in the USA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
3,440
Related Recalls
6
0 from same agency
Product description
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Bottle with pump, NET WT 16 fluid oz / 473.17 ml, Made in USA, www.painwizard.com Pain Wizard LLC.PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00012 3
Reason for recall
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0520-2024 |
| Date reported | June 5, 2024 |
| Date initiated | April 17, 2024 |
| Recalling firm | Arg Laboratories, Inc. |
| Firm location | Dallas, TX |
| Affected scope | 3,440 |
| Distribution | Distributed Nationwide in the USA |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0520-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Bottle with pump, NET WT 16 fluid oz / 473.17 ml, Made in USA, www.painwizard.com Pain Wizard LLC.PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00012 3. Recalled by Arg Laboratories, Inc.. Units affected: 3,440.
Why was this product recalled? ▼
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 5, 2024. Severity: Moderate. Recall number: D-0520-2024.
Where was the recalled product distributed? ▼
Distribution: Distributed Nationwide in the USA.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0520-2024) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported June 5, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.