SURGIMESH WN — Class II medical device recall Z-1986-2025
Completed recall by Chamberlain Technologies LLC, reported 2025-06-25, distributed in CA, IL, NE. Potential presence of residual adhesive material on the mesh surface.
| Recall number | Z-1986-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Chamberlain Technologies LLC, Deer Park, IL, United States |
| Recall initiated | 2022-08-12 |
| Classified | 2025-06-17 |
| Reported by FDA | 2025-06-25 |
| Distributed | CA, IL, NE |
| Quantity | 20 units |
| UPC / GTIN / UDI-DI | 00850011929155 |
| Lot numbers | Z2459757H |
| Model numbers | T1415 |
| Expiration dates | 2025-07-01 |
Product
SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415
Reason for recall
Potential presence of residual adhesive material on the mesh surface.
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-1986-2025. 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.