The Green Herb 100% Natural AL-ER-G — Class I food recall F-2291-2017
Terminated recall by MusclMasster, LLC, reported 2017-06-07, distributed in CO, SC, WA, WY. MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they contain the presence of Ephedra He
| Recall number | F-2291-2017 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MusclMasster, LLC, Wheat Ridge, CO, United States |
| Recall initiated | 2017-05-23 |
| Classified | 2017-06-01 |
| Reported by FDA | 2017-06-07 |
| Terminated | 2017-08-03 |
| Distributed | CO, SC, WA, WY |
| Lot numbers | 1892, 314 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-2291-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.