Class II — Chamberlain Technologies LLC
| Recalling firm | Chamberlain Technologies, LLC |
|---|---|
| Registered facility | CHAMBERLAIN TECHNOLOGIES, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Completed |
| Reason | Potential presence of residual adhesive material on the mesh surface. |
| Product | SURGIMESH XB, Polymeric Surgical Mesh, 14m x 15cm Flat Sheet with Silicone Barrier, Model/Catalog Number: Tintra R-1415 |
| Quantity | 20 units |
| Distribution | US distribution to states of: Illinois, Nebraska, & California |
| Initiated | 2022-08-12 |
| Classified | 2025-06-17 |
| Recall number | Z-1984-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Chamberlain Technologies LLC (Z-1984-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96930/
Alerts for Chamberlain Technologies, LLC
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.