# FDA recall D-66200-001

> **Fallon Wellness Pharmacy Llc** · Class II · drug recall initiated 2013-09-05.

## Product

Bevacizumab 25mg/mL, prepared as pre-filled syringes in 0.05 mL and 0.06 mL sizes, Fallon Wellness Pharmacy, Latham, NY 12110.

## Reason for recall

Lack of Assurance of Sterility: Fallon Pharmacy recalled Bevacizumab 25mg/mL due to sterility assurance concerns based on testing of this lot by a third party lab, indicating that test results reported as passing sterility may have been inaccurate.

## Distribution

NY & ME

## Key facts

- **Recall number:** D-66200-001
- **Recalling firm:** Fallon Wellness Pharmacy Llc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-09-05
- **Report date:** 2013-11-06
- **Termination date:** 2017-02-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Latham, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-66200-001

## Citation

> AI Analytics. FDA recall D-66200-001. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-66200-001. Source: US FDA. Licensed CC0.

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