The Recall Desk
ModerateFDA (Devices)·Z-1986-2025·Announced 2025-06-25

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.

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. 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
Hazard
Affected units
20

Distribution

Distributed in 3 states:

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 →

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