# FDA recall Z-1325-2025

> **Intuitive Surgical, Inc.** · Class II · device recall initiated 2025-02-26.

## Product

Brand Name: Da Vinci 5  Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals  Model/Catalog Number: 380730  Software Version: N/A  .     Refer to HHE for additional details.  Component: N/A

## Reason for recall

Due to an increase in complaints  concerning foot tray pedal spring failing resulting in the  pedal remaining pressed

## Distribution

Worldwide distribution - US Nationwide and the countries of Alaska, Arizona, Arkansas, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, 	South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, 	Wisconsin, Wyoming and the country of South Korea.

## Key facts

- **Recall number:** Z-1325-2025
- **Recalling firm:** Intuitive Surgical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-26
- **Report date:** 2025-03-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sunnyvale, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1325-2025

## Citation

> AI Analytics. FDA recall Z-1325-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1325-2025. Source: US FDA. Licensed CC0.

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