# FDA recall D-0109-2017

> **Teva Pharmaceuticals USA** · Class III · drug recall initiated 2016-09-22.

## Product

PARICALCITOL Capsules, 1 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD  21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA  19454, NDC 0093-7656-56.

## Reason for recall

Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-0109-2017
- **Recalling firm:** Teva Pharmaceuticals USA
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-09-22
- **Report date:** 2016-10-26
- **Termination date:** 2017-05-05

- **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-0109-2017

## Citation

> AI Analytics. FDA recall D-0109-2017. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0109-2017. Source: US FDA. Licensed CC0.

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