Chamberlain Technologies LLC: Medical Device Recall in 2025 - (Recall #: Z-1985-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 12, 2022

Date Posted: June 25, 2025

Recall Number: Z-1985-2025

Event ID: 96930

Reason for Recall:

Potential presence of residual adhesive material on the mesh surface.

Status: Ongoing

Product Quantity: 10 units

Code Information:

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

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated