Class II

Medical Device Recall: SURGIMESH XB, Polymeric Surgical Mesh, 14m x 15cm Flat Sheet with Silicone Barrier, Model/Catalog Number: Tintra R-1415

Chamberlain Technologies LLC · August 12, 2022

Reason for Recall

Potential presence of residual adhesive material on the mesh surface.

Distribution

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

Quantity Affected

20 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1984-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.