Koala Hand Sanitizer — Class II drug recall D-1357-2020
Terminated recall by Beaming White Llc, reported 2020-07-08, distributed nationwide. Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isoprop
| Recall number | D-1357-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beaming White Llc, Vancouver, WA, United States |
| Recall initiated | 2020-06-12 |
| Classified | 2020-06-26 |
| Reported by FDA | 2020-07-08 |
| Terminated | 2024-03-11 |
| Distributed | Nationwide (US) |
| Reason classes | undeclared allergen, labeling, potency |
| Lot numbers | 40820 |
| Expiration dates | 2023-04-08 |
Product
Koala Hand Sanitizer, Soothing Eucalyptus, 16 FL OZ., Antibacterial, (Ethyl Alcohol 68%), 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1357-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.