Surgical Mesh Recalled Due to Residual Adhesive Material Concern
Chamberlain Technologies LLC is recalling SURGIMESH WN polymeric surgical mesh due to potential residual adhesive material on the mesh surface. The recall affects 20 units distributed to 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. The source text does not report any illnesses, injuries, or adverse events; the hazard is theoretical (potential residual material), and no confirmed harm has occurred. This meets the criteria for a moderate severity rating.
Plain-English summary
Chamberlain Technologies LLC is recalling SURGIMESH WN, a polymeric surgical mesh (Model/Catalog Number T1415, 14cm x 15cm flat sheet), due to the potential presence of residual adhesive material on the mesh surface. The recall involves 20 units with Lot Number Z2459757H and an expiration date of July 1, 2025.
The affected product was distributed to medical facilities in Illinois, Nebraska, and California. Consumers or healthcare providers who have this product should stop using it and contact the manufacturer for further instructions.
The recalled product
- Product
- SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415
- Manufacturer
- Chamberlain Technologies LLC
- Category
- Medical Device — Surgical Mesh
- Affected units
- 20
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 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
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