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
- Affected units
- 60
Distribution
Part of a larger recall action
This product is one of 4 recalled by Chamberlain Technologies LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 4 products in this recall →Related recalls
Same manufacturer · Chamberlain Technologies LLC
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FDA (Devices) · 2025-06-25
- ModerateSurgical Mesh Product Recalled Due to Residual Adhesive Material
FDA (Devices) · 2025-06-25
- ModerateSurgical Mesh Recalled Due to Residual Adhesive Material Concern
FDA (Devices) · 2025-06-25