June 2021 FDA Recall Drug by Prairie Wolf Spirits
D-0694-2021 - Hand sanitizer packaged in bottles that resemble beverage containers.

This Class I drug recall was voluntarily initiated by Prairie Wolf Spirits on June 21, 2021 for the product Drug. The FDA reported the reason for recall as hand sanitizer packaged in bottles that resemble beverage containers.. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0694-2021

Reason for Recall
Hand sanitizer packaged in bottles that resemble beverage containers.
Initiated
06-21-2021
Reported
07-21-2021
Quantity
Unknown

Recall Profile & Regulatory Data

Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Prairie Wolf Spirits
Nationwide in the US
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

Batch or Lot Expiration Information

Lot# All lots