Biotin Solution for Injection — Class II drug recall D-0261-2022
Terminated recall by ASP CARES, reported 2021-12-08. Lack of Assurance of Sterility
| Recall number | D-0261-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ASP CARES, San Antonio, TX, United States |
| Recall initiated | 2021-11-17 |
| Classified | 2021-11-26 |
| Reported by FDA | 2021-12-08 |
| Terminated | 2022-12-02 |
| Quantity | 896 vials |
| Reason classes | sterility |
| NDC | 72833-0589-30 |
| Lot numbers | 091721589 |
| Expiration dates | 2022-03-16 |
Product
Biotin Solution for Injection, 10 mg/mL, 30 mL Multiple Dose Vial, Sterile, For IM or IV use only, Rx only ASP Cares, 2414 Babcock Rd Ste #106, San Antonio, TX 78229 NDC 72833-0589-30
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-0261-2022. 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.