The Recall Desk
ModerateFDA (Devices)·Z-1983-2025·Announced 2025-06-25

Surgical Mesh Recalled for Potential Residual Adhesive Material

Chamberlain Technologies LLC is recalling SURGIMESH WN Polymeric Surgical Mesh due to potential residual adhesive material on the mesh surface. The 60-unit recall affects medical facilities in Illinois, Nebraska, and California.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: This is an FDA Class II recall with no reported illnesses or injuries. The hazard is residual adhesive material, which is a manufacturing/quality defect rather than a high-risk pathogen or known adverse health consequence, placing it at the Moderate level per the rubric.

Plain-English summary

Chamberlain Technologies LLC is recalling SURGIMESH WN Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number T3030, due to the potential presence of residual adhesive material on the mesh surface.

This is a Class II recall of 60 units distributed to medical facilities in Illinois, Nebraska, and California. The affected lot is Lot Number Z2459757F (Expiration Date: July 1, 2025; UDI: (01)00850011929186(17)250701(10)Z2459757F).

Medical professionals who have received this product should contact Chamberlain Technologies LLC regarding the recall. Any patient or healthcare provider who has concerns about a product they may have received should consult with their physician or appropriate healthcare provider.

The recalled product

Product
SURGIMESH WN, Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number: T3030
Manufacturer
Chamberlain Technologies LLC
Category
Medical Device — Surgical Mesh
Hazard
  • residual-adhesive-material
  • manufacturing-defect

Distribution

Distribution scope not specified by the agency.

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