# FDA recall D-0922-2018

> **La Vita Compounding Pharmacy, LLC** · Class II · drug recall initiated 2018-06-25.

## 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.

## Distribution

Product was distributed to patients via patient specific prescription only in CA.

## Key facts

- **Recall number:** D-0922-2018
- **Recalling firm:** La Vita Compounding Pharmacy, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-06-25
- **Report date:** 2018-07-25
- **Termination date:** 2019-01-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0922-2018

## Citation

> AI Analytics. FDA recall D-0922-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0922-2018. Source: US FDA. Licensed CC0.

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