The Recall Desk
SevereFDA (Drugs)·D-1358-2020·Announced 2020-07-08

Koala Hand Sanitizer Recalled for Subpotent Ethanol and Undeclared Isopropyl Alcohol

Beaming White LLC is recalling Koala Hand Sanitizer because the active ingredient ethanol was tested below the label claim and undeclared isopropyl alcohol was present.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class II, which corresponds to a Severe severity score under the rubric for significant injury or property damage reports or high-risk contamination.

Plain-English summary

Beaming White LLC is voluntarily recalling specific lots of Koala Hand Sanitizer, Menthol, 16 FL OZ., Antibacterial. The recall is due to the active ingredient ethanol being tested below the label claim and the presence of undeclared isopropyl alcohol.

The affected product is distributed nationwide within the United States. The recall includes lots 40920, 41320, 41420, 41620, 41720, and 41720-2, with expiration dates ranging from April 9, 2023, to April 17, 2023.

Consumers should stop using the recalled product and contact the manufacturer for further instructions or a refund.

The recalled product

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

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (12)

  • 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

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 3 recalled by Beaming White Llc under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 3 products in this recall →

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