CLASS I Drug recall · Reported 21 Jul 2021 · FDA Enforcement Report
Prairie Wolf Distillery Alcohol Antiseptic recalled
Prairie Wolf Spirits is recalling Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer, distributed nationwide in the US. The recall was initiated on 21 Jun 2021 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0694-2021
- FDA event ID
- 88156
- Recalling firm
- Prairie Wolf Spirits, Guthrie, OK
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 21 Jun 2021
- FDA classified
- 22 Jul 2021
- Reported
- 21 Jul 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Packaging Defects
- Drug class
- Creams, Ointments & Gels
Timeline
| 21 Jun 2021 | Recall initiated by company | |
| 21 Jul 2021 | Published in enforcement report | +30 days |
| 22 Jul 2021 | Classified by FDA | +1 day |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Hand sanitizer packaged in bottles that resemble beverage containers.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
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
Where it was distributed
Nationwide in the US
Questions about this recall
Is Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer recalled?
Yes. Prairie Wolf Spirits recalled Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer on 21 Jun 2021. The recall is Class I and its status is Terminated. Recall number D-0694-2021.
Why was it recalled?
Hand sanitizer packaged in bottles that resemble beverage containers.
Which lots are affected?
All lots
Where was it sold?
Nationwide in the US
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.