SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
Reported: June 25, 2025 Initiated: August 12, 2022 #Z-1985-2025
Product Description
SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
Reason for Recall
Potential presence of residual adhesive material on the mesh surface.
Details
- Recalling Firm
- Chamberlain Technologies LLC
- Units Affected
- 10 units
- Distribution
- US distribution to states of: Illinois, Nebraska, & California
- Location
- Deer Park, IL
Frequently Asked Questions
What product was recalled? ▼
SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030. Recalled by Chamberlain Technologies LLC. Units affected: 10 units.
Why was this product recalled? ▼
Potential presence of residual adhesive material on the mesh surface.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 25, 2025. Severity: Moderate. Recall number: Z-1985-2025.
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