Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Topical Products

Beaming White Llc: Koala Hand Sanitizers Recalled for Low Alcohol Content and Undeclared Ingredients

Agency Publication Date: June 26, 2020
Share:
Sign in to monitor this recall

Summary

Beaming White LLC has recalled several varieties of Koala Hand Sanitizer (Soothing Eucalyptus, Menthol, and Unscented) because the active ingredient, ethanol, was found to be at levels lower than what is stated on the label. Additionally, the products contain undeclared isopropyl alcohol, which was not listed as an ingredient. These 16-ounce bottles were distributed nationwide within the United States.

Risk

Subpotent hand sanitizer may not effectively kill germs, bacteria, or viruses on the hands, providing a false sense of security during use. The presence of undeclared isopropyl alcohol also means consumers are using a product with ingredients they did not expect and that were not properly vetted for the labeled formula.

What You Should Do

  1. Check your 16-ounce bottle of Koala Hand Sanitizer for the following lot numbers and expiration dates: Lot 40820 (Exp. 4/8/23) for Soothing Eucalyptus; Lots 40920, 41320, 41420, 41620, 41720, or 41720-2 (Exp. dates between 4/9/23 and 4/17/23) for Menthol; or Lot 42220 (Exp. 4/22/23) for Unscented.
  2. Stop using the affected hand sanitizer immediately if you identify a matching lot number.
  3. Contact your healthcare provider or pharmacist if you have concerns regarding the effectiveness of the product or if you have experienced any adverse reactions.
  4. Return any unused product to the place of purchase for a refund and contact Beaming White LLC for further instructions.
  5. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Return product to place of purchase

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Koala Hand Sanitizer, Soothing Eucalyptus (16 FL OZ.)
Model:
Recall #: D-1357-2020
Lot Numbers:
40820 (Exp. Date 4/8/23)
Date Ranges: Exp. Date 4/8/23
Product: Koala Hand Sanitizer, Menthol (16 FL OZ.)
Model:
Recall #: D-1358-2020
Lot Numbers:
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 (Exp. Date 4/17/23)
41720-2 (Exp. Date 4/17/23)
Date Ranges: 4/9/23, 4/13/23, 4/14/23, 4/16/23, 4/17/23
Product: Koala Hand Sanitizer, Unscented (16 FL OZ.)
Model:
Recall #: D-1359-2020
Lot Numbers:
42220 (Exp. Date 4/22/23)
Date Ranges: Exp. Date 4/22/23

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85784
Status: Resolved
Manufacturer: Beaming White Llc
Manufactured In: United States
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.