Intuitive Surgical recalls da Vinci S/Si reusable cautery hook instruments with frayed or broken pitch cables that could cause injury during surgery. Affected models include 420183.
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
Intuitive Surgical is recalling da Vinci S and Si reusable cautery hook instruments due to reports of frayed or broken pitch cables. This could lead to injury during surgical procedures if the cables fail while in use.
The pitch cables in these instruments can fray or break during use, potentially causing the instrument to malfunction. If the cable fails while in use, it could lead to injury to the patient or the surgical team.
Surgical teams using da Vinci S or Si systems with the specific model 420183 cautery hooks are affected. Surgeons and surgical staff who use these instruments during procedures are at risk.
Check if your da Vinci S or Si system has the model number 420183 on the cautery hook. The instrument is part of the reusable surgical tools used in endoscopic procedures.
Inspect the cautery hook for frayed or broken pitch cables. If found, stop using it immediately.
Reach out to Intuitive Surgical for guidance on next steps if you have the affected model.
Due to increased complaints about frayed or broken pitch cables on reusable surgical instruments.
The model number 420183 for da Vinci S/Si permanent cautery hook instruments.
Check if your da Vinci S or Si system has the model number 420183 on the cautery hook.
We’ve drafted a message you can send Intuitive Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1701-2026 — Intuitive Surgical Intuitive Surgical Hello, I own a Intuitive Surgical that is covered by recall Z-1701-2026 from Intuitive Surgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.