Deer Park, IL, United States
Chamberlain Technologies LLC recalls
1 recall recorded since 2018, most recently on 12 August 2022. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Completed Class II Medical devices
- Recall started
- 12 August 2022
- Reason
- Potential presence of residual adhesive material on the mesh surface.
- Distribution
- US distribution to states of: Illinois, Nebraska, & California
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1986-2025, Z-1985-2025, Z-1983-2025, Z-1984-2025
- SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415
- SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
- SURGIMESH WN, Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number: T3030
- SURGIMESH XB, Polymeric Surgical Mesh, 14m x 15cm Flat Sheet with Silicone Barrier, Model/Catalog Number: Tintra R-1415
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.