FDA recall D-0694-2021

Prairie Wolf Spirits · Class I · drug

Product

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.

Distribution

Nationwide in the US

Key facts

Status
Terminated
Initiation date
2021-06-21
Report date
2021-07-21
Termination date
2023-10-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
Guthrie, OK, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0694-2021