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Medium risk Drugs & MedicationsClass II

Intuitive Surgical, Inc. Recall

Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Nu

Updated December 9, 2025

Intuitive Surgical, Inc. is recalling Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Nu. Hazard: Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments

Is the Intuitive Surgical, Inc. recalled? Yes. This product was recalled by FDA on December 9, 2025. Details below.

What is recalled

Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Product Description: EndoWrist Instruments or da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use. All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient). Component: NA

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments

Brands affected

Intuitive Surgical, Inc.
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-1701-2026
Classification
Class II
Recalled
December 9, 2025
Read the official notice

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