# FDA recall D-0694-2021

> **Prairie Wolf Spirits** · Class I · drug recall initiated 2021-06-21.

## 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.

## Distribution

Nationwide in the US

## Key facts

- **Recall number:** D-0694-2021
- **Recalling firm:** Prairie Wolf Spirits
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-06-21
- **Report date:** 2021-07-21
- **Termination date:** 2023-10-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Guthrie, OK, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0694-2021

## Citation

> AI Analytics. FDA recall D-0694-2021. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0694-2021. Source: US FDA. Licensed CC0.

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