Ready to Use Thymo-Cide — Class II medical device recall Z-0358-2014
Terminated recall by Wexford Labs Inc, reported 2013-11-27, distributed nationwide. Expired active ingredient was used in the manufacture of the product.
| Recall number | Z-0358-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wexford Labs Inc, Kirkwood, MO, United States |
| Recall initiated | 2013-09-10 |
| Classified | 2013-11-19 |
| Reported by FDA | 2013-11-27 |
| Terminated | 2014-04-23 |
| Distributed | Nationwide (US) |
| Lot numbers | 0109131, 0215131, 0320131, 0415132, 0516131, 0624131, 091721, 10/13, 101521, 11/13, 2/14, 3/14, 4/14, 5/14, 6/14, 7/14 |
Product
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.
Reason for recall
Expired active ingredient was used in the manufacture of the product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0358-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.