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Class II: temporary or reversible health riskOngoing

ARG Laboratories Pain Wizard Recall

Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), E…

ARG Laboratories, Inc. · Dallas, TX

Risk level
Class II
Reported by FDA
Jun 5, 2024
Recall ID
D-0520-2024
Check your lot numberHow we source this data

Summary

ARG Laboratories recalled Pain Wizard starting Apr 17, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0520-2024 on Jun 5, 2024. Reason: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process. Status: Ongoing.

Why it was recalled

Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

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

Lot numbers, UPCs & expiration codes

Lot: 18723C3, Exp 06/30/2025

Where it was sold

Distributed Nationwide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0520-2024
Classification
Class II
Status
Ongoing
Recall initiated
Apr 17, 2024
FDA report date
Jun 5, 2024
Quantity
3,440
Recall type
Voluntary: Firm initiated
Recalling firm
ARG Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-0520-2024, exactly as published.

Show all FDA fields
City
Dallas
State
TX
Status
Ongoing
Country
United States
Event ID
94354
Address
2639 Manana Dr
Code information
Lot: 18723C3, Exp 06/30/2025
Postal code
75220-1301
Report date
Jun 5, 2024
Product type
Drugs
Recall number
D-0520-2024
Classification
Class II
Recalling firm
ARG Laboratories, Inc.
Product quantity
3,440
Reason for recall
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
Distributed Nationwide in the USA
Recall initiation date
Apr 17, 2024
Initial firm notification
Letter
Center classification date
May 30, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0520-2024, published Jun 5, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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