Z-1983-2025 Class II
FDA device recall Z-1983-2025 was initiated by Chamberlain Technologies LLC on August 12, 2022 and is designated Class II. Reason for recall: Potential presence of residual adhesive material on the mesh surface. Affected quantity: 60 units.
Recall Details
- Product Type
- Devices
- Report Date
- June 25, 2025
- Initiation Date
- August 12, 2022
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 60 units
Product Description
SURGIMESH WN, Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number: T3030
Reason for Recall
Potential presence of residual adhesive material on the mesh surface.
Distribution Pattern
US distribution to states of: Illinois, Nebraska, & California
Code Information
Lot Code: Reference Number: T3030 UDI: (01)00850011929186(17)250701(10)Z2459757F Lot Number: Z2459757F Expiration Date: 2025-07-01