Methyl Folate CA+ 1mg/ml Injection w/Pres — Class II drug recall D-0922-2018
Terminated recall by La Vita Compounding Pharmacy, LLC, reported 2018-07-25, distributed in CA. Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug
| Recall number | D-0922-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | La Vita Compounding Pharmacy, LLC, San Diego, CA, United States |
| Recall initiated | 2018-06-25 |
| Classified | 2018-07-13 |
| Reported by FDA | 2018-07-25 |
| Terminated | 2019-01-18 |
| Distributed | CA |
| Quantity | 17,610 ml |
| Reason classes | sterility |
| Expiration dates | 2018-08-06, 2018-09-03, 2018-09-24, 2018-10-22, 2018-11-12 |
Product
Methyl Folate CA+ 1mg/ml Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), 10 mL and 30 mL vials, Rx only, la VITA Compounding Pharmacy, 858.453.2500
Reason for recall
Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
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-0922-2018. 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.