FDA Enforcement Class II Ongoing

SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030

Recall: Z-1985-2025 · Reported June 25, 2025

Enforcement

Recall Number
Z-1985-2025
Event ID
96930
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Chamberlain Technologies LLC
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
June 25, 2025
Initiation Date
August 12, 2022
Classification Date
June 17, 2025
Address
21805 W Field Pkwy, N/A, Deer Park, IL, 60010-3228, United States

Description

SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030

Reason

Potential presence of residual adhesive material on the mesh surface.

Code Info

Lot Code: Reference Number: Tintra E-3030 UDI: (01)00850011929063(17)250701(10)Z2459757G Lot Number: Z2459757G Expiration Date: 2025-07-01

Distribution

US distribution to states of: Illinois, Nebraska, & California

Quantity

10 units