# FDA recall D-809-2013

> **Mobius Therapeutics LLC** · Class I · drug recall initiated 2013-01-03.

## Product

Mitosol (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use (NDC 49771-002-01), 3 kits per box (NDC 49771-002-03), Rx only, Manufactured for: Mobius Therapeutics, LLC, 4041 Forest Park Avenue, St. Louis, MO  63108 USA.

## Reason for recall

Non-Sterility: one or more components of the kit have been found to be contaminated with yeast.

## Distribution

Nationwide and Military and Government Consignees

## Key facts

- **Recall number:** D-809-2013
- **Recalling firm:** Mobius Therapeutics LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-01-03
- **Report date:** 2013-07-31
- **Termination date:** 2013-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Louis, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-809-2013

## Citation

> AI Analytics. FDA recall D-809-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-809-2013. Source: US FDA. Licensed CC0.

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