Class ITerminated in FDA datasetRecall initiated May 23, 2017

The Green Herb 100% Natural AL-ER-G, 60 and 150 Capsules, Dietary supplement, This item is…

Recalling firm: MusclMasster, LLC

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 3, 2017.

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ProductThe 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.

FDA code information

All manufactured.

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Full FDA record and distribution details

Original product description

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.

Extracted codes and context

TypeCode / valueContext
batch1892150 capsules, each capsule is 180 mg of ephedra herb in a 650 mg capsule. Batch#1892; product# 314.

Original FDA recall reason

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

Recall details

Recall number
F-2291-2017
Event ID
77358
FDA status
Terminated
Initiated
May 23, 2017
Reported
Jun 7, 2017
Classified
Jun 1, 2017
Terminated
Aug 3, 2017
Quantity
Unknown
Location
Wheat Ridge, CO, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

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

FDA source record · F-2291-2017

Data updated September 16, 2026. View official FDA data ↗

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