# FDA recall D-0004-2018

> **Inopak Ltd** · Class II · drug recall initiated 2017-08-23.

## Product

Choice Antibacterial Hand Soap, (ethyl alcohol 61%)  800 ml/ 27 fl oz, Universal Valve,  Inopak LTD, Ringwood, NJ

## Reason for recall

GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump.

## Distribution

nationwide

## Key facts

- **Recall number:** D-0004-2018
- **Recalling firm:** Inopak Ltd
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-08-23
- **Report date:** 2017-10-11
- **Termination date:** 2020-04-20

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0004-2018

## Citation

> AI Analytics. FDA recall D-0004-2018. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0004-2018. Source: US FDA. Licensed CC0.

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