Chamberlain Technologies recalls SURGIMESH XB surgical mesh due to potential residual adhesive on the mesh surface. Affected units include specific model and lot numbers. Consumers should contact the company for details.
Potential presence of residual adhesive material on the mesh surface.
Chamberlain Technologies is recalling SURGIMESH XB polymeric surgical mesh that may have residual adhesive material on the surface. This could pose a risk during medical procedures or post-surgery recovery.
Residual adhesive material on the mesh surface could cause irritation or complications during surgery or after the procedure. This may lead to adverse reactions in patients.
Patients who received this surgical mesh during procedures between 2023 and 2025 are likely affected. Medical professionals using the mesh for surgeries are also at risk.
Check for the model number Tintra R-1415 on the mesh product. The lot number Z2459695M and expiration date of July 1, 2025 are also specific identifiers.
Reach out to Chamberlain Technologies for specific guidance on whether your mesh is affected and next steps.
The recall indicates potential residual adhesive, but the product is not unsafe for use unless the adhesive causes complications during surgery or recovery.
Look for the model number Tintra R-1415 and lot number Z2459695M on the mesh product.
Contact Chamberlain Technologies directly to determine if your specific mesh is affected and follow their instructions.
We’ve drafted a message you can send Chamberlain Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1984-2025 — Chamberlain Technologies Chamberlain Technologies Hello, I own a Chamberlain Technologies that is covered by recall Z-1984-2025 from Chamberlain Technologies. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.