Methylcobalamin — Class II drug recall D-417-2013
Terminated recall by NuVision Pharmacy, Inc., reported 2013-05-22, distributed in FL, MO, UT, WA. Lack of Assurance of Sterility; reports of adverse events after injection
| Recall number | D-417-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | NuVision Pharmacy, Inc., Dallas, TX, United States |
| Recall initiated | 2013-03-28 |
| Classified | 2013-05-16 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2016-10-19 |
| Distributed | FL, MO, UT, WA |
| Quantity | 32 vials |
| Reason classes | sterility |
Product
Methylcobalamin (Buffered) Injection,1 mg/mL, 30 mL vial, Stock# 11126, Preservative Free, Compounded by NuVision Pharmacy, Inc., Dallas, TX 75244
Reason for recall
Lack of Assurance of Sterility; reports of adverse events after injection
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-417-2013. 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.