Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1701-2026 — 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 dis

U.S. FDA — Device Enforcement · United States · 2025-12-09 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1701-2026
Date of alert: 2025-12-09
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Intuitive Surgical, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00886874111536

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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