HIGHFDA DEVICE

Intuitive Surgical da Vinci S/Si Monopolar Curved Scissors Recall for 86,904 Units Worldwide (2025)

Intuitive Surgical recalled 86,904 da Vinci S and Si Monopolar Curved Scissors instruments sold worldwide to hospitals and surgical centers. The recall cites increased complaints of broken or frayed grip cables on reusable instruments. Healthcare facilities should stop using the device immediately and follow the manufacturer’s recall instructions.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
December 9, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
December 9, 2025
Hazard Level
HIGH
Brand
Intuitive Surgical
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Intuitive Surgical
Product type
da Vinci S/Si Monopolar Curved Scissors Instrument
Model numbers
420179-10, 420179-12, 420179-14, 420179-15, 420179
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    December 9, 2025

  2. Reported by FDA DEVICE

    April 8, 2026

  3. RecallRadar source check

    April 15, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Due to increased complaints for broken/frayed grip cables for reusable instruments.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Intuitive Surgical, Inc. or your healthcare provider for instructions. Notification method: Letter

About This Product

The da Vinci S/Si Monopolar Curved Scissors are EndoWrist instruments used in robotic-assisted surgery for tissue manipulation, dissection and cautery. They are reusable and rely on mechanical grip cables to transmit motion.

Why This Is Dangerous

The recall cites increased complaints of broken or frayed grip cables. Such faults can compromise instrument control during procedures.

Industry Context

This recall is not described as part of a broader industry pattern in the provided data.

Real-World Impact

Hospitals may need to substitute instruments, potentially delaying procedures and increasing coordination with suppliers for replacements.

Practical Guidance

How to identify if yours is affected

  1. Verify instrument is a da Vinci S/Si Monopolar Curved Scissors with Model 420179
  2. Check for batch/lot codes and GTINs listed in recall documentation
  3. Cross-check material numbers 420179-10, -12, -14, -15 on the instrument label

Where to find product info

Model number and batch codes printed on instrument label; GTIN and material number on packaging

What timeline to expect

Refunds/replacements typically take weeks to months per recall process

If the manufacturer is unresponsive

  • Escalate with hospital procurement and regulatory agencies
  • Document all communications and dates of contact

How to prevent similar issues

  • Verify instrument serials before use
  • Maintain records of instrument batch histories
  • Coordinate with the manufacturer for compliant replacements

Documentation advice

Retain recall notice, purchase receipts if available, serial numbers, batch/lot codes, photos of the instrument label and packaging

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

Product: da Vinci S/Si Monopolar Curved Scissors Instrument Model/Catalog Numbers: 420179, 420179-10, 420179-12, 420179-14, 420179-15 Where Sold: Worldwide distribution to hospitals and surgical centers Sold Since: Unknown Price: Unknown

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Worldwide distribution to hospitals and surgical centers
  • Hazard: broken/frayed grip cables
  • No reported injuries or incidents

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
420179-10
420179-12
420179-14
420179-15
420179
Affected States
ALL
Report Date
April 8, 2026
Recall Status
ACTIVE

Related Recalls

Health & Personal Care
HIGH

Intuitive Surgical Recalls da Vinci 5 Display Over High Injury Risk

Intuitive Surgical recalled 47 da Vinci 5 Surgeon Console Viewer Displays on December 30, 2025. The devices may lose display functionality, risking surgical injury. Healthcare providers should stop using the consoles immediately and follow recall instructions.

Intuitive Surgical
Robotic-assisted surgical
Read more