Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Terminated Initiated Jun 21, 2021 (5 years ago)

Prairie Wolf Distillery Alcohol Antiseptic 80%

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Hand sanitizer packaged in bottles that resemble beverage containers.

Cause type: Packaging defect

Failed child-resistant closures, leaks, cracked containers, or a defective delivery device. Packaging failures risk accidental exposure (especially to children) or product contamination. All packaging defect recalls.

What was recalled

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

Affected NDCs 73891-0100-14 73891-0100-15

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Drug: Alcohol

Recalling firm
Prairie Wolf Spirits
Origin
OK, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0694-2021 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Alcohol recalls

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Other packaging defect recalls from 2021

All packaging defect recalls
Class II · Moderate risk

Brinzolamide Ophthalmic Suspension

Defective Container: The notch in the cap that fits into the nozzle of the dropper could break off and block the dropper possibly resulting in the product not dispensing.

Terminated Packaging defect Teva Pharmaceuticals USA NDC 0591-2127-79 D-0373-2022
Class II · Moderate risk

Diclofenac Sodium Topical Solution

Defective container: Out of specification for container integrity leading to bottles leaking.

Ongoing Packaging defect Preferred Pharmaceuticals, Inc. NDC 68788-7707-01 D-0278-2022