Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 88156

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 21, 2021
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Prairie Wolf Spirits

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

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

D-0694-2021
Recall number
D-0694-2021
Initiated
June 21, 2021
Classification
Class I
Status
Terminated
Recalling firm
Prairie Wolf Spirits
Quantity
Unknown

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Hand sanitizer packaged in bottles that resemble beverage containers.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Hand sanitizer packaged in bottles that resemble beverage containers.

Code information

All lots

Distribution pattern

Nationwide in the US