Prairie Wolf Spirits recalls Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer, packaged in a) (16.9oz) 500 mL (UPC 8…

Recall date

June 21, 2021

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0694-2021

FDA classification

Class I

Brand / firm

Prairie Wolf Spirits

Sold / distributed

Nationwide in the US

Why it was recalled

Hand sanitizer packaged in bottles that resemble beverage containers.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer, packaged in a) (16.9oz) 500 mL (UPC 8 60003 31899 7, NDC: 73891-100-14); and b) (20oz) 591 mL (UPC 8 60003 65984 7 NDC: 73891-100-15) bottles, Prairie Wolf Distillery, Guthrie, Oklahoma