# FDA recall D-1439-2014

> **Teva Pharmaceuticals USA** · Class III · drug recall initiated 2014-06-17.

## Product

Velivet (desogestrel and ethinyl estradiol tablets - triphasic regimen),   0.1 mg/0.025 mg; 0.125 mg/0.025 mg; 0.15 mg/0.025 mg, 3 Dispensers x 28 Tablets, Barr Laboratories, Inc., Pomona, NY  NDC 0555-9051-67

## Reason for recall

Failed Impurities/Degradation Specifications: out of specification impurity test results.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1439-2014
- **Recalling firm:** Teva Pharmaceuticals USA
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-06-17
- **Report date:** 2014-07-23
- **Termination date:** 2015-03-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** North Wales, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1439-2014

## Citation

> AI Analytics. FDA recall D-1439-2014. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1439-2014. Source: US FDA. Licensed CC0.

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