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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66391

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

Open FDA event record

Event summary

Timeline bucket
September 10, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Wexford Labs Inc

Dossier provenance

Source snapshots represented here

  • openFDA Device 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.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

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.

device · product 1 of 1

Ready to Use Thymo-Cide, Germicidal Detergent, containing 0.051% thymol, packaged in 1-qt. bottles. The firm name on the label is Wexford Labs, Inc., Kirkwood, MO. For disinfection of hard, non-porous surfaces (floors, walls, tables, etc.) in operating rooms, intensive care, nurseries, emergency areas, dental operatories, police, EMS, and all health care facilities.

Z-0358-2014
Recall number
Z-0358-2014
Initiated
September 10, 2013
Classification
Class II
Status
Terminated
Recalling firm
Wexford Labs Inc
Quantity
7,020/1-qt. bottles (1755 gallons)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Expired active ingredient was used in the manufacture of the product.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Expired active ingredient was used in the manufacture of the product.

Code information

Lot numbers 091721, exp. 10/13; 101521, exp. 11/13; 0109131, exp. 2/14; 0215131, exp. 3/14; 0320131, exp. 4/14; 0415132, exp. 5/14; 0516131, exp. 6/14; and 0624131, 7/14.

Distribution pattern

Nationwide Distribution - USA including FL, SC, TX, MO, CA, OH, OK, MA, IN, and GA.