---
title: "SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Ca... — FDA record Z-1985-2025 | Is It on Recall"
description: "Potential presence of residual adhesive material on the mesh surface."
url: https://isitonrecall.com/recall/fda-device-z-1985-2025-surgimesh-xb-polymeric-surgical-mesh-x-large-ellipse-barrier-mesh-model-catalog-number-tintra-e-3030/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030 — FDA record Z-1985-2025

Reported completed

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 12, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
- **Reason**: Potential presence of residual adhesive material on the mesh surface.
- **Classification**: Class II
- **Recalling firm**: Chamberlain Technologies LLC
- **Quantity**: 10 units
- **Agency-reported status**: Completed
- **Source record identifier**: Z-1985-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1985-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot Code: Reference Number: Tintra E-3030 UDI: (01)00850011929063(17)250701(10)Z2459757G Lot Number: Z2459757G Expiration Date: 2025-07-01 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US distribution to states of: Illinois, Nebraska, & California

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)

## Dates in the source

- **Report date**: Jun 25, 2025
- **Recall initiation date**: Aug 12, 2022
- **Center classification date**: Jun 17, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1985-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Chamberlain Technologies LLC records](https://isitonrecall.com/brand/chamberlain-technologies-llc/)