Methylcobalamin 10 mg/mL Injection — Class II drug recall D-1478-2019
Terminated recall by First Pharma Associates LLC dba Riverpoint Pharmacy, reported 2019-07-17, distributed in ID, WA. Lack of Assurance of Sterility.
| Recall number | D-1478-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | First Pharma Associates LLC dba Riverpoint Pharmacy, Spokane, WA, United States |
| Recall initiated | 2019-06-26 |
| Classified | 2019-07-11 |
| Reported by FDA | 2019-07-17 |
| Terminated | 2023-06-06 |
| Distributed | ID, WA |
| Quantity | 5.4 ml |
| Reason classes | sterility |
| Expiration dates | 2019-08-19 |
Product
Methylcobalamin 10 mg/mL Injection, 5.4 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.
Reason for recall
Lack of Assurance of Sterility.
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-1478-2019. 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.