# FDA recall D-1114-2017

> **C. O. Truxton** · Class II · drug recall initiated 2017-04-20.

## Product

Phenobarbital Tablets USP, 100 mg, a) 100 count bottles (NDC 0463-6152-01), b) 1000 count bottles (NDC 0163-6152-10), Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031

## Reason for recall

Labeling: Label Mixup; potentially mislabeled

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1114-2017
- **Recalling firm:** C. O. Truxton
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-04-20
- **Report date:** 2017-08-30
- **Termination date:** 2018-09-11

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1114-2017

## Citation

> AI Analytics. FDA recall D-1114-2017. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1114-2017. Source: US FDA. Licensed CC0.

---

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