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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96960

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

Open FDA event record

Event summary

Timeline bucket
May 23, 2025
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Consumer Product Partners, LLC

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

Spectrum Advanced Gel Hand Sanitizer, Ethyl alcohol 70%, 8 FL OZ (236 mL) per bottle, Manufactured for Medline Industries, Inc., Three Lakes Drive, Northfield, IL 60693 USA. NDC: 53329-202-08, UPC 8 88277 34945 5

D-0458-2025
Recall number
D-0458-2025
Initiated
May 23, 2025
Classification
Class II
Status
Ongoing
Quantity
125,040 bottles

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Subpotent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol

Code information

Lot, expiry: Lot 0644682, exp 2026/11/14; Lot 0644683, exp 2026/11/16

Distribution pattern

Nationwide in the USA.

Field note

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