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RECALL RECORD — CLASS IRecall closedF-2291-2017/FDA enforcement
Musclmasster, LLC·Dietary Supplements·May 23, 2017

The Green Herb 100% Natural Al-er-g, 60 and 150 Capsules, Dietary Supplement, This Item Is…

What you need to know

Class I

  • What happened

    MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they contain the presence of Ephedra Herb, an FDA banned ingredient.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. 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 FDACO, WY, SC, WA +2 moreMore supplements

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Product identification

Source: FDA FOOD

Brand nameMusclmasster, LLC
Recalling firmMusclmasster, LLCWheat Ridge, CO, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • All manufactured.
Distribution area
COWYSCWAORVA

Distributed to CO, WY, SC, WA. No foreign or govt/VA/military consignees.

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: June 7, 2017
FDA recall numberF-2291-2017

Beyond the headline

The recall, in context

Musclmasster, LLC initiated this supplements recall on May 23, 2017. The FDA enforcement report states: MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they contain the presence of Ephedra Herb, an FDA banned ingredient. The FDA report lists distribution as: Distributed to CO,WY,SC,WA. No foreign or govt/VA/military consignees.

The FDA enforcement report describes the reason as: MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they contain the presence of Ephedra Herb, an FDA banned ingredient.

The Green Herb 100% Natural Al-er-g, 60 and 150 Capsules, Dietary Supplement, This Item Is… was made or distributed by Musclmasster, LLC in Wheat Ridge, CO, United States. This page reflects FDA report F-2291-2017, dated June 7, 2017.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

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 lot and date codes 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 The Green Herb 100% Natural Al-er-g, 60 and 150 Capsules, Dietary Supplement, This Item Is… recall?

Musclmasster, LLC recalled The Green Herb 100% Natural Al-er-g, 60 and 150 Capsules, Dietary Supplement, This Item Is… in an FDA Class I enforcement action reported as F-2291-2017. MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they contain the presence of Ephedra Herb, an FDA banned ingredient.

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 Musclmasster, LLC 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-2291-2017. 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

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