# FDA recall D-1350-2015

> **Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals** · Class III · drug recall initiated 2015-08-13.

## Product

AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee, NJ, By: Suir Pharma Ireland Ltd., Clonmel, Ireland, NDC:  67253-180-50

## Reason for recall

Labeling: Incorrect Or Missing Package Insert: Product is labeled with unapproved labeling.

## Distribution

U.S. Including: OH

## Key facts

- **Recall number:** D-1350-2015
- **Recalling firm:** Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-08-13
- **Report date:** 2015-08-26
- **Termination date:** 2015-08-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Huntsville, AL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1350-2015

## Citation

> AI Analytics. FDA recall D-1350-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1350-2015. Source: US FDA. Licensed CC0.

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