# FDA recall D-0008-2017

> **West-Ward Pharmaceutical** · Class II · drug recall initiated 2016-10-03.

## Product

PredniSONE Tablets USP, 1 mg, 100-count bottles, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ  07724, NDC 0054-4741-25.

## Reason for recall

Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.

## Distribution

US Nationwide.

## Key facts

- **Recall number:** D-0008-2017
- **Recalling firm:** West-Ward Pharmaceutical
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-10-03
- **Report date:** 2016-10-12
- **Termination date:** 2017-12-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Columbus, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0008-2017

## Citation

> AI Analytics. FDA recall D-0008-2017. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-0008-2017. Source: US FDA. Licensed CC0.

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