FDA Device recall Z-1054-2016
Milex Arcing Diaphragm Size 95
- FDA Device
- Class II
- terminated
- Published 2016-03-16
On 2016-03-16 the FDA classified a Class II recall of Milex Arcing Diaphragm Size 95 by Coopersurgical, citing the products have been identified to contain an incorrect size Diaphragm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1054-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-02-16 |
| Published | 2016-03-16 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Coopersurgical |
| Distribution | NY, OR |
Product
Milex Arcing Diaphragm Size 95; Model Number: MXWS95
Reason
The products have been identified to contain an incorrect size Diaphragm.
Identifiers
| code_info | Lot# 130438 |
|---|
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-1054-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.