# FDA recall D-0147-2017

> **West-Ward Pharmaceuticals Corp.** · Class III · drug recall initiated 2016-11-04.

## Product

Amoxicillin for Oral suspension, USP 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by: Hikma Pharmaceuticals, P.O. Box 183400, Amman 11118 - Jordan, NDC 0143-9887-01

## Reason for recall

Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0147-2017
- **Recalling firm:** West-Ward Pharmaceuticals Corp.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-11-04
- **Report date:** 2016-11-30
- **Termination date:** 2017-06-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Eatontown, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0147-2017

## Citation

> AI Analytics. FDA recall D-0147-2017. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0147-2017. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
