Lower risk Drug recall · FDA · Published June 21, 2021

Prairie Wolf Spirits Hand Sanitizer Recall: Risk of Confusion with Beverages

Prairie Wolf Spirits recalls 80% alcohol hand sanitizer bottles that look like beverage containers to prevent accidental ingestion by children.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0694-2021Drug Prairie Wolf Spirits ›

Lower-risk recall

Hand sanitizer packaged in bottles that resemble beverage containers.

Take action

Contact the company

Recalling firmPrairie Wolf Spirits124 E Oklahoma Ave · Guthrie, OK 73044-3243

✎ GovInfoNow plain-language explainer

Prairie Wolf Spirits is recalling hand sanitizer products that are packaged in bottles resembling beverage containers. This recall is to prevent accidental ingestion by children who might mistake the product for a drink. Read more at govinfonow.com/recall/36113-prairie-wolf-spirits-hand-sanitizer-recall-risk-of-confusion-with.

Source Summary by GovInfoNow · govinfonow.com/recall/36113-prairie-wolf-spirits-hand-sanitizer-recall-risk-of-confusion-with · Updated August 18, 2026 · FDA enforcement record: FDA #D-0694-2021

Cite this page

“Prairie Wolf Spirits Hand Sanitizer Recall: Risk of Confusion with Beverages.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/36113-prairie-wolf-spirits-hand-sanitizer-recall-risk-of-confusion-with. Based on FDA recall #D-0694-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0694-2021%22&limit=1).

The FDA announced on June 21, 2021, that Prairie Wolf Spirits recalled hand sanitizer because the packaging resembles beverage containers, posing an ingestion hazard. The agency classified the recall as Class I.

How to tell if you have it

Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer
UPC 8 60003 31899 7 (16.9oz / 500 mL)
UPC 8 60003 65984 7 (20oz / 591 mL)

The hazard

The hand sanitizer is packaged in bottles that resemble beverage containers, creating a risk of accidental ingestion. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show Zep issued a recall for Alcohol Sanitizer Spray on May 22, 2026, due to microbial contamination risk. American Regent recalled ACETYLCYSTEINE Solution and Tralement injection on July 24, 2026, citing particulate matter hazards.

How to tell if you have this one

Check for bottles labeled 'Prairie Wolf Distillery Alcohol Antiseptic 80%'. The products come in 16.9oz (500 mL) and 20oz (591 mL) sizes with specific UPC and NDC numbers.

Brand
Prairie Wolf Spirits
Product
Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer, packaged in a) (16.9oz) 500 mL (UPC 8
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the product name and size on the bottle to confirm it's the recalled hand sanitizer.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Nationwide in the US” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.3 years after the firm started it.

Jun 21, 2021Firm started the recall
Jul 21, 2021Published in FDA’s Enforcement Report
Jul 22, 2021FDA classified it Class I
Oct 16, 2023FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/36113-prairie-wolf-spirits-hand-sanitizer-recall-risk-of-confusion-with">Prairie Wolf Spirits Hand Sanitizer Recall: Risk of Confusion with Beverages (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0694-2021 (June 21, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0694-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.