Milex Arcing Diaphragm Size 95 — Class II medical device recall Z-1054-2016
Terminated recall by CooperSurgical, Inc., reported 2016-03-16, distributed in NY, OR. The products have been identified to contain an incorrect size Diaphragm.
| Recall number | Z-1054-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2016-02-16 |
| Classified | 2016-03-04 |
| Reported by FDA | 2016-03-16 |
| Terminated | 2016-03-29 |
| Distributed | NY, OR |
| Quantity | 2 units |
| Lot numbers | 130438 |
| Model numbers | MXWS95 |
Product
Milex Arcing Diaphragm Size 95; Model Number: MXWS95
Reason for recall
The products have been identified to contain an incorrect size Diaphragm.
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-1054-2016. 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.