# FDA recall D-140-2013

> **Hillyard GMP** · Class II · drug recall initiated 2012-12-28.

## Product

HILLYARD, Alcohol Free Foaming Instant Hand Sanitizer, Benzalkonium Chloride 0.10%, 1.25 L plastic bottle, OTC, HILLYARD IDUSTRIES, St. Joseph, MO. 64502 NDC 76402-403-03

## Reason for recall

Microbial Contamination of Non-Sterile Products: The product may be contaminated with bacteria.

## Distribution

Distribution nationwide

## Key facts

- **Recall number:** D-140-2013
- **Recalling firm:** Hillyard GMP
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-12-28
- **Report date:** 2013-02-06
- **Termination date:** 2014-01-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Joseph, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-140-2013

## Citation

> AI Analytics. FDA recall D-140-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-140-2013. Source: US FDA. Licensed CC0.

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