Killz Germz Hand Sanitizer Recalled for Sub-Potent Alcohol Levels
Genesis Partnership Company SA is recalling Killz Germz Hand Sanitizer because testing showed ethanol levels as low as 62%, below the labeled 70% claim.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity score. The hazard involves sub-potent alcohol levels, which is a labeling/potency issue rather than a direct physical injury risk like choking or fire, and no illnesses or injuries are reported in the source text.
Plain-English summary
Genesis Partnership Company SA is recalling 5,320 bottles of Killz Germz Hand Sanitizer, Alcohol Gel, 450 mL (15 fl oz.). The product was manufactured in Guatemala for Killz Germz, LLC., in Washington, DC.
The recall was initiated due to sub-potent results. Testing revealed that ethanol levels in the product were as low as 62%, while the label claims 70% alcohol content. The affected lots are 36748, 36818, and 36697, with expiration dates of 10/15/21 and 11/8/21.
The product was distributed nationwide in the U.S. Consumers should check their inventory for these specific lot numbers and expiration dates. If found, the product should be returned to the place of purchase or disposed of according to local regulations.
The recalled product
- Product
- Killz Germz Hand Sanitizer, Alcohol Gel, 450 mL (15 fl oz.) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, For: Killz Germz, LLC., 1912 R street NW, Washington DC, 20009, NDC 74625-003-04, UPC 7401037203250.
- Manufacturer
- Genesis Partnership Company SA
- Category
- Drug — Hand Sanitizer
- Affected units
- 5,320
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 (4)
- Lot #s: 36748
- 36818
- 36697
- Exp. 10/15/21 and 11/8/21
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 5 recalled by Genesis Partnership Company SA 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 5 products in this recall →Related recalls
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