---
title: "AURORA Surgiscope System. Sterile, single use device that contains a Sheath, ... — FDA record Z-2331-2024 | Is It on Recall"
description: "Potential sheath damage that could lead to tissue damage and/or track hemorrhage."
url: https://isitonrecall.com/recall/fda-device-z-2331-2024-aurora-surgiscope-system-sterile-single-use-device-that-contains-a-sheath-obturator-and-imager/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# AURORA Surgiscope System. Sterile, single use device that contains a Sheath, Obturator, and Imager. — FDA record Z-2331-2024

Reported ongoing

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 Jun 7, 2024. 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**: AURORA Surgiscope System. Sterile, single use device that contains a Sheath, Obturator, and Imager.
- **Reason**: Potential sheath damage that could lead to tissue damage and/or track hemorrhage.
- **Classification**: Class II
- **Recalling firm**: Integra LifeSciences Corp.
- **Quantity**: 14 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2331-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2331-2024%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 | Model No. ASX9/130; UDI# 00850002332278; Lot No. 7336314. |

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

## Distribution

Domestic: NY, OH, & DC.

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

- [District of Columbia](https://isitonrecall.com/state/district-of-columbia/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)

## Dates in the source

- **Report date**: Jul 17, 2024
- **Recall initiation date**: Jun 7, 2024
- **Center classification date**: Jul 10, 2024

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-2331-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Integra LifeSciences Corp. records](https://isitonrecall.com/brand/integra-lifesciences-corp/)