CLASS I Food recall · Reported 7 Jun 2017 · FDA Enforcement Report

The Green Herb 100% Natural Al-er recalled by MusclMasster

MusclMasster is recalling The Green Herb 100% Natural Al-er-g, 60 and, Dietary supplement, This, distributed in Colorado, South Carolina, Virginia, Washington, Wyoming. The recall was initiated on 23 May 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll manufactured.

Quantity recalledUnknown

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-2291-2017
FDA event ID: 77358
Recalling firm: MusclMasster, Wheat Ridge, CO
Classification: Class I
Status: Terminated
Recall initiated: 23 May 2017
FDA classified: 1 Jun 2017
Reported: 7 Jun 2017
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Other Reasons
Product category: Dietary Supplements

Timeline

23 May 2017	Recall initiated by company
1 Jun 2017	Classified by FDA	+9 days
7 Jun 2017	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

The Green Herb 100% Natural AL-ER-G, 60 and 150 Capsules, Dietary supplement, This item is packed in a white bottle with a white cap. Each bottle contains 60 or 150 capsules, each capsule is 180 mg of ephedra herb in a 650 mg capsule. Batch#1892; product# 314.

Where it was distributed

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

Colorado South Carolina Virginia Washington Wyoming

Questions about this recall

Why was it recalled?

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

Which lots are affected?

All manufactured.

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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