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RecallFDAfda-F-1931-2013MISLABELED

MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX GOUT AID***Dietary Supplement 130 Tablets***6 0 65176 26512 ...

Category
Units Affected
2,245
Recall Date
June 10, 2013
Issuing Agency
Hazard
Mislabeled

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1931-2013.

In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1931-2013.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Healthmaxx Global Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1931-2013.

Healthmaxx Global Inc.

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Healthmaxx Global Inc. Recall FAQ

Healthmaxx Global Inc. is the subject of a supplements safety report: MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX GOUT AID***Dietary Supplement 130 Tablets***6 0 65176 26512 .... The notice was published on June 10, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 2,245 units are potentially affected.