# FDA recall D-842-2013

> **Teva Pharmaceuticals USA, Inc.** · Class II · drug recall initiated 2013-07-23.

## Product

Terazosin Hydrochloride Capsules,10 mg, 100-count bottle, Rx only, Manufactured for Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-4339-01

## Reason for recall

Labeling -label error on declared strength: unopened, sealed bottle of Terazosin Hydrochloride (HCl) 10mg Capsules contained Terazosin HCl 5 mg Capsules

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-842-2013
- **Recalling firm:** Teva Pharmaceuticals USA, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-07-23
- **Report date:** 2013-08-14
- **Termination date:** 2014-08-27

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-842-2013

## Citation

> AI Analytics. FDA recall D-842-2013. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-842-2013. Source: US FDA. Licensed CC0.

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