FDA Food recall · Reported June 7, 2017
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.
MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they contain the presence of Ephedra Herb, an FDA banned ingredient.
MusclMasster, LLC recalled The Green Herb 100% Natural AL-ER-G, 60 and 150 Capsules, Dietary supplement, This item i… - a critical-severity action.
The Green Herb 100% Natural AL-ER-G, 60 and 150 Capsules, Dietary supplement, This item i… was recalled by MusclMasster, LLC in June 7, 2017. Reason: MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they contain the presence of Ephedra H…. Check the official notice for the remedy. Verify recall #F-2291-2017 with the FDA Food before acting.
The recall
MusclMasster, LLC issued this critical-severity FDA Food recall-MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they contain the presence of Ephedra H….
- Critical
- severity level
- Class I
- classification
- June 7, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2291-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,472 drugs & medications recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
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.
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-2291-2017 |
| Date reported | June 7, 2017 |
| Date initiated | May 23, 2017 |
| Recalling firm | MusclMasster, LLC |
| Firm location | Wheat Ridge, CO |
| Affected scope | Unknown |
| Distribution | Distributed to CO,WY,SC,WA. No foreign or govt/VA/military consignees. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-2291-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Nationwide recalls with similar severity or category timing
Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Critical), closest by report date among other firms and states.
Similar Drugs & Medications · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026