RecallRadar

FDA Drug recall D-0694-2021

Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer, packaged in a) (16.9oz) 500 mL (UPC 8 60003 31899 7, NDC:…

On 2021-07-21 the FDA classified a Class I recall of Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer, packaged in a) (16.9oz) 500 mL (UPC 8 60003 31899 7, NDC:… by Prairie Wolf Spirits, citing hand sanitizer packaged in bottles that resemble beverage containers.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0694-2021
ClassificationClass I
Statusterminated
Initiated2021-06-21
Published2021-07-21
Last updated2026-09-13 11:52 UTC
CompanyPrairie Wolf Spirits
DistributionUS

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

Hand sanitizer packaged in bottles that resemble beverage containers.

Identifiers

upc860003318997
upc860003659847
code_infoAll lots

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0694-2021%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.