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

Recall Z-1432-2013 — 8mm Maryland Bipolar Forceps used in conjunction with the da Vinci Surgical System, Model IS1200. Multiple use electrosurgical endoscopic instruments.

U.S. FDA — Device Enforcement · United States · 2013-05-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1432-2013
Date of alert
2013-05-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Intuitive Surgical, Inc.
Product category
device
Product type
Devices
Reported risk: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug Riser, preventing a bipolar cautery cable from being properly connected which results in loss of cautery function of Bipolar 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.

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