# FDA recall D-1358-2020

> **Beaming White Llc** · Class II · drug recall initiated 2020-06-12.

## Product

Koala Hand Sanitizer, Menthol, 16 FL OZ.,  Antibacterial, (Ethyl Alcohol 69%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665

## Reason for recall

Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-1358-2020
- **Recalling firm:** Beaming White Llc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2020-06-12
- **Report date:** 2020-07-08
- **Termination date:** 2024-03-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Vancouver, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1358-2020

## Citation

> AI Analytics. FDA recall D-1358-2020. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-1358-2020. Source: US FDA. Licensed CC0.

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