Prairie Wolf Distillery Alcohol Antiseptic 80% — Class I drug recall D-0694-2021
Terminated recall by Prairie Wolf Spirits, reported 2021-07-21, distributed nationwide. Hand sanitizer packaged in bottles that resemble beverage containers.
| Recall number | D-0694-2021 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Prairie Wolf Spirits, Guthrie, OK, United States |
| Recall initiated | 2021-06-21 |
| Classified | 2021-07-22 |
| Reported by FDA | 2021-07-21 |
| Terminated | 2023-10-16 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 00860003318997, 00860003659847 |
| NDC | 73891-0100-14, 73891-0100-15 |
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
Reason for recall
Hand sanitizer packaged in bottles that resemble beverage containers.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0694-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.