---
title: "Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for mi... — FDA record Z-1428-2026 | Is It on Recall"
description: "An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or t"
url: https://isitonrecall.com/recall/fda-device-z-1428-2026-da-vinci-5-assy-dv5-console-is5000-model-catalog-number-380730-used-for-minimally-invasive-surgery/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery. — FDA record Z-1428-2026

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 Nov 17, 2025. 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**: Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery.
- **Reason**: An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower monitor.
- **Classification**: Class II
- **Recalling firm**: Intuitive Surgical, Inc.
- **Quantity**: 12
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1428-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1428-2026%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 | UDI-DI: 00886874119747 GTIN: 0886874119747 with software version P1.2.1 |

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

## Distribution

US distribution: LA, MA, NY, PA, TX, and VA.

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

- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: Feb 25, 2026
- **Recall initiation date**: Nov 17, 2025
- **Center classification date**: Feb 18, 2026

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-1428-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Intuitive Surgical, Inc. records](https://isitonrecall.com/brand/intuitive-surgical-inc/)