# FDA recall D-1354-2014

> **Teva Pharmaceuticals USA** · Class II · drug recall initiated 2014-03-21.

## Product

ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY

## Reason for recall

Non-sterility: due to a failed sterility test

## Distribution

NY and KY

## Key facts

- **Recall number:** D-1354-2014
- **Recalling firm:** Teva Pharmaceuticals USA
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-03-21
- **Report date:** 2014-06-04
- **Termination date:** 2014-11-14

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1354-2014

## Citation

> AI Analytics. FDA recall D-1354-2014. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-1354-2014. Source: US FDA. Licensed CC0.

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