# FDA recall D-0248-2025

> **Turbare Manufacturing** · Class II · drug recall initiated 2025-02-18.

## Product

Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not for Resale - Single Use, This drug product was repackaged by Turbare Manufacturing, 925 Jeanette Drive, Conway, AR 72032, NDC: 83556-0101-01.

## Reason for recall

Lack of Assurance of Sterility: due to a quality control process deviation

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0248-2025
- **Recalling firm:** Turbare Manufacturing
- **Classification:** Class II
- **Product type:** drug
- **Status:** Completed
- **Initiation date:** 2025-02-18
- **Report date:** 2025-03-05
- **Termination date:** 2026-02-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Conway, AR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0248-2025

## Citation

> AI Analytics. FDA recall D-0248-2025. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-0248-2025. Source: US FDA. Licensed CC0.

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