CaviWipes1 Extra Large — Class II medical device recall Z-1402-2017
Terminated recall by Metrex Research, LLC., reported 2017-03-15, distributed nationwide. Metrex is recalling the CaviWipes Extra Large because they may have been contaminated during the packaging pro
| Recall number | Z-1402-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Metrex Research, LLC., Romulus, MI, United States |
| Recall initiated | 2017-01-20 |
| Classified | 2017-03-03 |
| Reported by FDA | 2017-03-15 |
| Terminated | 2017-09-01 |
| Distributed | Nationwide (US) |
| Quantity | 960 cases |
| Lot numbers | 16-2340PA |
| Model numbers | 13-5150 |
Product
CaviWipes1 Extra Large, Part No. 13-5150 The brand name of the device is CaviWipes1 Extra Large, a surface disinfectant. The device has been assigned the product code LRJ (General Purpose Disinfectant) by the FDA and is classified as a Class I Medical Device. CaviWipes1 Extra Large is intended to be used to disinfect surfaces.
Reason for recall
Metrex is recalling the CaviWipes Extra Large because they may have been contaminated during the packaging process.
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-1402-2017. 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.