Chamberlain recalls X-Large Ellipse Barrier Mesh (Tintra E-3030) due to potential residual adhesive on the mesh surface. Affected units have specific lot numbers and expiration dates.
Potential presence of residual adhesive material on the mesh surface.
Chamberlain is recalling a specific type of surgical mesh product due to a potential risk of residual adhesive material on the mesh surface. This could pose a risk during medical procedures or after implantation.
Residual adhesive material could potentially cause irritation or complications during or after surgical procedures. This risk is specific to the mesh product and not a general hazard for all surgical mesh types.
Patients who received or are scheduled to receive the Chamberlain SURGIMESH XB X-Large Ellipse Barrier Mesh (Tintra E-3030) model with the lot number Z2459757G are affected. Medical professionals using this product for surgical procedures may also be impacted.
Check for the model number Tintra E-3030 on the product packaging. Affected units have the lot number Z2459757G and expire by July 1, 2025.
Look for the model number Tintra E-3030 and lot number Z2459757G on the product packaging.
This recall applies to specific surgical mesh products. If you received the Tintra E-3030 model with lot number Z2459757G, contact your surgeon for guidance.
Check for the model number Tintra E-3030 and lot number Z2459757G on the product packaging. Affected units expire by July 1, 2025.
The recall does not require immediate action. Check the product details and contact your healthcare provider for further instructions.
We’ve drafted a message you can send Chamberlain to request your refund or repair — edit it as you like.
Subject: Recall Z-1985-2025 — Chamberlain Chamberlain Hello, I own a Chamberlain that is covered by recall Z-1985-2025 from Chamberlain. 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.
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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.
