CLASS II Drug recall · Reported 8 Jul 2020 · FDA Enforcement Report
Koala Hand Sanitizer, Menthol, Antibacterial, (Ethyl Alcohol 69%) recalled
Beaming White is recalling Koala Hand Sanitizer, Menthol, Antibacterial, (Ethyl Alcohol 69%), distributed nationwide in the US. The recall was initiated on 12 Jun 2020 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1358-2020
- FDA event ID
- 85784
- Recalling firm
- Beaming White, Vancouver, WA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Jun 2020
- FDA classified
- 26 Jun 2020
- Reported
- 8 Jul 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Labeling Errors
- Drug class
- Hand Sanitizer
Timeline
| 12 Jun 2020 | Recall initiated by company | |
| 26 Jun 2020 | Classified by FDA | +14 days |
| 8 Jul 2020 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.
Product as listed by the FDA
Koala Hand Sanitizer, Menthol, 16 FL OZ., Antibacterial, (Ethyl Alcohol 69%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665
Where it was distributed
Nationwide within the United States
Questions about this recall
Is Koala Hand Sanitizer, Menthol, Antibacterial, (Ethyl Alcohol 69%) recalled?
Yes. Beaming White recalled Koala Hand Sanitizer, Menthol, Antibacterial, (Ethyl Alcohol 69%) on 12 Jun 2020. The recall is Class II and its status is Terminated. Recall number D-1358-2020.
Why was it recalled?
Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.
Which lots are affected?
Lot #: 40920, Exp. Date 4/9/23; 41320, Exp. Date 4/13/23; 41420, Exp, Date 4/14/23; 41620, Exp. Date 4/16/23; 41720, 41720-2, Exp. Date 4/17/23
Where was it sold?
Nationwide within the United States
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Beaming White
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Koala Hand Sanitizer, Unscented, Antibacterial, (Ethyl Alcohol 70%) recalled | Beaming White | Labeling Errors | Nationwide |
| Drug | CLASS II | Koala Hand Sanitizer, Soothing Eucalyptus, Antibacterial recalled | Beaming White | Labeling Errors | Nationwide |