PlainRecalls
FDA Drug Critical Class I Terminated

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

Reported: July 21, 2021 Initiated: June 21, 2021 #D-0694-2021

Product Description

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

Reason for Recall

Hand sanitizer packaged in bottles that resemble beverage containers.

Details

Recalling Firm
Prairie Wolf Spirits
Units Affected
Unknown
Distribution
Nationwide in the US
Location
Guthrie, OK

Frequently Asked Questions

What product 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. Recalled by Prairie Wolf Spirits. Units affected: Unknown.
Why was this product recalled?
Hand sanitizer packaged in bottles that resemble beverage containers.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 21, 2021. Severity: Critical. Recall number: D-0694-2021.