L-glutamine 30mg/ml 30ml vial — Class II drug recall D-157-2014
Terminated recall by Main Street Family Pharmacy, LLC, reported 2013-12-11, distributed nationwide. The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to compo
| Recall number | D-157-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Main Street Family Pharmacy, LLC, Newbern, TN, United States |
| Recall initiated | 2013-05-28 |
| Classified | 2013-12-03 |
| Reported by FDA | 2013-12-11 |
| Terminated | 2014-04-22 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
Product
L-glutamine 30mg/ml 30ml vial, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
Reason for recall
The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to compounded preservative-free methylprednisolone 80mg/ml 10 ml vials.
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/D-157-2014. 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.