FDA Device recall Z-1402-2017
CaviWipes1 Extra Large, Part No. 13-5150 The brand name of the device is CaviWipes1 Extra Large, a surface disinfectant
- FDA Device
- Class II
- terminated
- Published 2017-03-15
On 2017-03-15 the FDA classified a Class II recall of CaviWipes1 Extra Large, Part No. 13-5150 The brand name of the device is CaviWipes1 Extra Large, a surface disinfectant by Metrex Research, citing metrex is recalling the CaviWipes Extra Large because they may have been contaminated during the packaging process.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1402-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-01-20 |
| Published | 2017-03-15 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Metrex Research |
| Distribution | US |
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
Metrex is recalling the CaviWipes Extra Large because they may have been contaminated during the packaging process.
Identifiers
| code_info | Lot No. 16-2340PA |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1402-2017%22
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