---
title: "Signia\" Small Diameter Curved Tip Intelligent Reload, Model SIGSDS30CTVT — FDA record Z-1457-2024 | Is It on Recall"
description: "Under certain firing conditions, reloads were found to articulate in an uncontrolled manner potentially causing disruption to the staple line. The issue is rela"
url: https://isitonrecall.com/recall/fda-device-z-1457-2024-signia-small-diameter-curved-tip-intelligent-reload-model-sigsds30ctvt/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Signia" Small Diameter Curved Tip Intelligent Reload, Model SIGSDS30CTVT — FDA record Z-1457-2024

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 Feb 14, 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**: Signia" Small Diameter Curved Tip Intelligent Reload, Model SIGSDS30CTVT
- **Reason**: Under certain firing conditions, reloads were found to articulate in an uncontrolled manner potentially causing disruption to the staple line. The issue is related to components in impacted reloads that are not fully secure, which leads to uncontrolled articulation. The issue can occur using either the Endo GIA" Ultra Universal Stapler or Signia" Stapling System.
- **Classification**: Class II
- **Recalling firm**: Covidien, LP
- **Quantity**: 30 Units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1457-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1457-2024%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 Number: SIGSDS30CTVT; UDI/DI: 10884521741881; Lot number: N3L1909UY; |

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

## Distribution

Worldwide distribution - US Nationwide and the countries of France, Hong Kong, Israel and Japan.

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

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## Dates in the source

- **Report date**: Apr 10, 2024
- **Recall initiation date**: Feb 14, 2024
- **Center classification date**: Apr 1, 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-1457-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Covidien, LP records](https://isitonrecall.com/brand/covidien-lp/)