# FDA recall D-0155-2018

> **Solco Healtcare US LLC** · Class II · drug recall initiated 2017-12-04.

## Product

Gabapentin Tablets, USP, 800 mg, 500-count, Rx only, Made in India, PONDRUGS/16 134193, Distributed by: Solco Healthcare US, LLC, Cranbury, NJ, 08512, USA. NDC 43547-0333-50

## Reason for recall

Labeling: Label Mix-Up.some bottles labeled as Gabapentin 800 mg contain Gabapentin 600 mg

## Distribution

Product was distributed  in Mason, OH.

## Key facts

- **Recall number:** D-0155-2018
- **Recalling firm:** Solco Healtcare US LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-12-04
- **Report date:** 2018-01-17
- **Termination date:** 2019-02-25

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0155-2018

## Citation

> AI Analytics. FDA recall D-0155-2018. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/D-0155-2018. Source: US FDA. Licensed CC0.

---

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