FDAFDA · Food and drugs·Recall number 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: 73891-100-14); and b) (20oz) 591 mL (UPC 8 60003 65984 7 NDC: 73891-100-15) bottles, Prairie Wolf Distillery, Guthrie, Oklahoma
Published July 21, 2021 · Recall initiated: June 21, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Hand sanitizer packaged in bottles that resemble beverage containers.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Prairie Wolf Spirits
- Distributor
- Nationwide in the US
- Lot
- All lots
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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