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Use caution Medical device recall · FDA · Published February 26, 2025

Da Vinci 5 Foot Tray Pedals Recall: Pedal Stuck Due to Spring Failure

Intuitive Surgical recalls Da Vinci 5 foot tray pedals with model 380730 manufactured before December 20, 2024. Pedals may stay pressed causing discomfort or injury during surgery.

🇺🇸 FDA recall #Z-1325-2025Medical deviceIntuitive Surgical ›
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Recalling firmIntuitive Surgical, Inc.1266 Kifer Rd · Sunnyvale, CA 94086-5304
✎ GovInfoNow plain-language explainer

Intuitive Surgical is recalling Da Vinci 5 foot tray pedals with model number 380730 made before December 20, 2024. The pedals may stay pressed due to a spring failure, which could cause discomfort or injury during surgical procedures. Read more at govinfonow.com/recall/52740-da-vinci-5-foot-tray-pedals-recall-pedal-stuck-due.

Source Summary by GovInfoNow · govinfonow.com/recall/52740-da-vinci-5-foot-tray-pedals-recall-pedal-stuck-due · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1325-2025

Cite this page

“Da Vinci 5 Foot Tray Pedals Recall: Pedal Stuck Due to Spring Failure.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52740-da-vinci-5-foot-tray-pedals-recall-pedal-stuck-due. Based on FDA recall #Z-1325-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1325-2025%22&limit=1).

The FDA announced on Feb. 26, 2025, that Intuitive Surgical, Inc. is recalling Da Vinci 5 ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals due to a hazard where the pedal spring may fail and remain pressed. The recall affects 439 units distributed worldwide.

How to tell if you have it

  • Brand: Da Vinci 5
  • Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals
  • Model/Catalog Number: 380730
  • UDI: 00886874119747
  • Units manufactured prior to 12/20/2024

The hazard

The recall is due to an increase in complaints concerning foot tray pedal spring failing, resulting in the pedal remaining pressed. The record does not report specific incidents or injuries.

Context

GovInfoNow's records show Intuitive Surgical, Inc. has 53 other recalls on record since 2017-06-01. Other recent recalls of similar products include Da Vinci 5 dV5 Tower NIR Handheld Camera Recall (2026-04-24) and Intuitive Surgical Da Vinci Surgical System Recall (2026-04-22).

How to tell if you have this one

Check if your Da Vinci 5 console has model number 380730 and was manufactured before December 20, 2024. The pedals may feel stuck or remain pressed.

  • Brand
    Intuitive Surgical
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Pedal Condition

    Inspect if the foot tray pedals feel stuck or remain pressed during use.

  2. Contact Manufacturer

    Reach out to Intuitive Surgical for guidance on whether your specific model needs replacement.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA 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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 21 days after the firm started it.

1. Firm started the recall: Feb 26, 202512. FDA classified it Class II: Mar 12, 202523. Published in FDA’s Enforcement Report: Mar 19, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-1325-2025 (February 26, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1325-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA