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.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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
See all →- HighSurgical Mesh Recalled for Potential Residual Adhesive Material
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
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