RegWardenFDA facility compliance records
Recall

Class II — Wexford Labs Inc

Recalling firmWEXFORD LABS, INC.
Registered facilityWEXFORD LABS, INC. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonExpired active ingredient was used in the manufacture of the product.
ProductReady 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.
Quantity7,020/1-qt. bottles (1755 gallons)
DistributionNationwide Distribution - USA including FL, SC, TX, MO, CA, OH, OK, MA, IN, and GA.
Initiated2013-09-10
Classified2013-11-19
Terminated2014-04-23
Recall numberZ-0358-2014
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Wexford Labs Inc (Z-0358-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/66391/

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