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RECALL RECORD — CLASS IIRecall closedF-1298-2013/FDA enforcement
F.h.g Corporation Dba Integrity Nutraceuticals·Dietary Supplements·Mar 14, 2013

Musclepharm Brand Combat Powder (R), Banana Cream, Natural and Artifical Flavors, Hybrid Series…

What you need to know

Class II

  • What happened

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

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANC, MD, ID, FL +10 moreMore supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameF.h.g Corporation Dba Integrity Nutraceuticals
Recalling firmF.h.g Corporation Dba Integrity NutraceuticalsSpring Hill, TN, United States
UPC / barcodes
7 36211 05057 1
Lot / date codes
  • Lot # 123732 027, Expiration date 02/2015
Distribution area
NCMDIDFLARPACACTCOILUTNJIAMS

NC, MD, ID, FL, AR, PA, CA, CT, CO, IL, UT, NJ, IA, MS, Australia, Cook Islands

United States, Australia

Quantity affected2427 units
Recall initiationFDA report date: April 17, 2013
FDA recall numberF-1298-2013

Beyond the headline

The recall, in context

F.h.g Corporation Dba Integrity Nutraceuticals initiated this supplements recall on March 14, 2013. The FDA enforcement report states: One lot of each product may have extraneous materials due to a problem on the packing line. The FDA report lists distribution as: NC, MD, ID, FL, AR, PA, CA, CT, CO, IL, UT, NJ, IA, MS, Australia, Cook Islands.

The FDA enforcement report describes the reason as: One lot of each product may have extraneous materials due to a problem on the packing line.

Musclepharm Brand Combat Powder (R), Banana Cream, Natural and Artifical Flavors, Hybrid Series… was made or distributed by F.h.g Corporation Dba Integrity Nutraceuticals in Spring Hill, TN, United States. This page reflects FDA report F-1298-2013, dated April 17, 2013.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Musclepharm Brand Combat Powder (R), Banana Cream, Natural and Artifical Flavors, Hybrid Series… recall?

F.h.g Corporation Dba Integrity Nutraceuticals recalled Musclepharm Brand Combat Powder (R), Banana Cream, Natural and Artifical Flavors, Hybrid Series… in an FDA Class II enforcement action reported as F-1298-2013. One lot of each product may have extraneous materials due to a problem on the packing line.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the F.h.g Corporation Dba Integrity Nutraceuticals recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1298-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by F.h.g Corporation Dba Integrity Nutraceuticals

View brand
Class II·

F.h.g Corporation Dba Integrity Nutraceuticals

Musclepharm Brand Combat Powder (R), Cookies 'N' Cream, Natural and Artifical Flavors, Hybrid…

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

NC, MD, ID +11 more +1 countriesSupplements

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.