# FDA recall D-1393-2019

> **Ecolab Inc** · Class III · drug recall initiated 2019-05-10.

## Product

QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz cans, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102-1390 USA, NDC 47593-490-82

## Reason for recall

Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.

## Distribution

U.S.A. Nationwide

## Key facts

- **Recall number:** D-1393-2019
- **Recalling firm:** Ecolab Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-05-10
- **Report date:** 2019-06-26
- **Termination date:** 2022-09-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1393-2019

## Citation

> AI Analytics. FDA recall D-1393-2019. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/D-1393-2019. Source: US FDA. Licensed CC0.

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