Surgimesh XB recall
SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
Why was Surgimesh XB recalled?
Potential presence of residual adhesive material on the mesh surface.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Code: Reference Number: Tintra E-3030 UDI: (01)00850011929063(17)250701(10)Z2459757G Lot Number: Z2459757G Expiration Date: 2025-07-01
- Product
- SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
- Recalling firm
- Chamberlain Technologies LLC
- Quantity
- 10 units
- Distribution
- US distribution to states of: Illinois, Nebraska, & California
- Recall date
- June 25, 2025
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)