Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

© 2026 Go Backs. All rights reserved.

Critical RiskFDA Drug
Medications & Supplements/Topical Products

Prairie Wolf Spirits: Alcohol Antiseptic 80% Hand Sanitizer Recalled for Beverage-Like Packaging

Agency Publication Date: July 13, 2021
Share:
Sign in to monitor this recall

Summary

Prairie Wolf Spirits is recalling all lots of their Alcohol Antiseptic 80% Topical Solution Hand Sanitizer because the packaging closely resembles water or beverage containers. The product is sold in 16.9-ounce (500 mL) and 20-ounce (591 mL) plastic bottles that could be mistaken for drinking water. Consumers should immediately stop using these products and contact a healthcare provider if they suspect accidental ingestion. This recall covers all units distributed nationwide in the United States.

Risk

The hand sanitizer is packaged in bottles that look like beverage containers, posing a serious risk of accidental ingestion. Swallowing alcohol-based hand sanitizer can lead to alcohol toxicity, which may cause symptoms such as nausea, vomiting, dizziness, or even death in severe cases.

What You Should Do

  1. Check your home for Prairie Wolf Distillery Alcohol Antiseptic 80% Topical Solution Hand Sanitizer in 16.9oz (500 mL) or 20oz (591 mL) bottles.
  2. Identify the 16.9oz bottles by UPC 8 60003 31899 7 and NDC 73891-100-14.
  3. Identify the 20oz bottles by UPC 8 60003 65984 7 and NDC 73891-100-15.
  4. Immediately stop using the product and keep it out of reach of children to prevent accidental ingestion.
  5. Contact your healthcare provider or pharmacist for guidance regarding use or accidental exposure.
  6. Return any unused product to the place of purchase for a refund and contact Prairie Wolf Spirits for further instructions.
  7. If you have questions, contact the FDA Consumer Complaint line at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

💰Full Refund

Healthcare provider consultation and pharmacy return

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer (16.9oz/500 mL)
Model:
NDC: 73891-100-14
UPC Codes:
860003318997
Lot Numbers:
All lots
Product: Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer (20oz/591 mL)
Model:
NDC: 73891-100-15
UPC Codes:
860003659847
Lot Numbers:
All lots

Product Images

Prairie Wolf Distillery Hand Sanitizer front label

Prairie Wolf Distillery Hand Sanitizer front label

Prairie Wolf Distillery Hand Sanitizer back label

Prairie Wolf Distillery Hand Sanitizer back label

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88156
Status: Resolved
Manufacturer: Prairie Wolf Spirits
Manufactured In: United States
Units Affected: Unknown
Distributed To: Nationwide
Agency Last Updated: July 22, 2021

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.