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
Hand sanitizer packaged in bottles that resemble beverage containers.
06-21-2021
07-21-2021
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.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
The firm responsible for the recall.
Prairie Wolf Spirits
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
General area of initial distribution.
Nationwide in the US
10-16-2023
Product Description About Product Description
Full technical description of the product.
Full technical description of the 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
Batch or Lot Expiration Information
Lot# All lots