Chamberlain recalls SURGIMESH WN surgical mesh (model T1415) due to potential residual adhesive on the surface. Affected units sold through specific lot numbers until July 2025.
Potential presence of residual adhesive material on the mesh surface.
Chamberlain is recalling a specific type of surgical mesh (SURGIMESH WN) because it may have residual adhesive material on its surface. This could pose a risk during medical procedures or after implantation.
Residual adhesive material on the mesh surface could potentially cause irritation or complications during surgery or after implantation. This is a minor risk that does not typically cause serious injury.
Surgical patients who received this specific mesh product during procedures between 2023 and : 2025. Medical professionals using this mesh for surgeries are most at risk.
Check for the model number T1415 on the mesh product. The lot number Z2459757H and expiration date of July 2025 are also associated with this recall.
Look for the model number T1415, lot number Z2459757H, and expiration date of July 2025 on the mesh product.
The recall states potential residual adhesive material on the mesh surface, which could cause minor irritation or complications during surgery or after implantation. This is a low-risk issue.
Check for the model number T1415, lot number Z2459757H, and expiration date of July 2025 on the mesh product.
The recall does not specify a remedy, so no action is required beyond checking if your product matches the recall details.
We’ve drafted a message you can send Chamberlain Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1986-2025 — Chamberlain Technologies Chamberlain Technologies Hello, I own a Chamberlain Technologies that is covered by recall Z-1986-2025 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.
