Vitamin B12 liquid 1000mcg/ml — Class II drug recall D-0402-2019
Terminated recall by Hiers Enterprises, LLC dba Northwest Compounding Pharmacy, reported 2019-01-09, distributed in OR. Lack of sterility assurance.
| Recall number | D-0402-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hiers Enterprises, LLC dba Northwest Compounding Pharmacy, Roseburg, OR, United States |
| Recall initiated | 2019-01-02 |
| Classified | 2019-01-27 |
| Reported by FDA | 2019-01-09 |
| Terminated | 2023-03-28 |
| Distributed | OR |
| Quantity | 150 ml |
| Reason classes | sterility |
| Expiration dates | 2019-01-14, 2019-01-16 |
Product
Vitamin B12 liquid 1000mcg/ml, RX, glass vial
Reason for recall
Lack of sterility assurance.
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-0402-2019. 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.