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Recall Observatory FDA recall evidence

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

D-0694-2021

June 21, 2021

Class I

Product summary

Firm
Prairie Wolf Spirits
Event
Event 88156
Status
Terminated
Classification
Class I
Quantity
Unknown
Official record key
drug-enforcement:D-0694-2021

Official wording

Reason: Hand sanitizer packaged in bottles that resemble beverage containers.

Code information: All lots

Distribution pattern: Nationwide in the US

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Hand sanitizer packaged in bottles that resemble beverage containers.