Hydroxocobalamin MDV 5 mg/mL — Class II drug recall D-1060-2013
Terminated recall by Northern New England Compounding Pharmacy LLC, reported 2013-09-25, distributed in CT. Lack of Assurance of Sterility: The pharmacy is recalling one lot of Hydroxocobalamin MDV 5mg/mL due to failed
| Recall number | D-1060-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Northern New England Compounding Pharmacy LLC, Littleton, NH, United States |
| Recall initiated | 2013-09-05 |
| Classified | 2013-09-17 |
| Reported by FDA | 2013-09-25 |
| Terminated | 2013-09-17 |
| Distributed | CT |
| Quantity | 1 vials |
| Reason classes | sterility |
| Expiration dates | 2013-11-03 |
Product
Hydroxocobalamin MDV 5 mg/mL (5,000 mcg/mL) Inj., 10 mL vial X 3, Eastern States Compounding Pharmacy, Littleton, NH 03561
Reason for recall
Lack of Assurance of Sterility: The pharmacy is recalling one lot of Hydroxocobalamin MDV 5mg/mL due to failed sterility results by a third party contract testing lab. Hence the sterility of the product cannot be assured.
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-1060-2013. 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.