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High RiskFDAfda-F-1297-2013FOREIGN MATERIAL

MUSCLEPHARM brand COMBAT POWDER (R), COOKIES 'N' CREAM, NATURAL AND ARTIFICAL FLAVORS, HYBRID SERIES DIETARY SUPPLEMENT, NET WEIGHT 2 LBS...

Category
Units Affected
2,541
Recall Date
March 14, 2013
Issuing Agency
Hazard
Foreign Material

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1297-2013.

One lot of each product may have extraneous materials due to a problem on the packing line.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1297-2013.

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 F.h.g Corporation Dba Integrity Nutraceuticals 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-1297-2013.

F.H.G Corporation dba Integrity Nutraceuticals

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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F.h.g Corporation Dba Integrity Nutraceuticals Recall FAQ

F.h.g Corporation Dba Integrity Nutraceuticals is the subject of a dairy safety report: MUSCLEPHARM brand COMBAT POWDER (R), COOKIES 'N' CREAM, NATURAL AND ARTIFICAL FLAVORS, HYBRID SERIES DIETARY SUPPLEMENT, NET WEIGHT 2 LBS.... The notice was published on March 14, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 2,541 units are potentially affected.