# FDA recall D-010-2013

> **Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals** · Class II · drug recall initiated 2012-10-11.

## Product

Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL  35811,  NDC 0603-5092-21.

## Reason for recall

Tablet Separation: Possibility of cracked or split coating on the tablets.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-010-2013
- **Recalling firm:** Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-10-11
- **Report date:** 2012-10-31
- **Termination date:** 2013-12-09

- **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-010-2013

## Citation

> AI Analytics. FDA recall D-010-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-010-2013. Source: US FDA. Licensed CC0.

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