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

Recall Z-2741-2017 — MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software defined spatial boundaries during orthopedic procedures.

U.S. FDA — Device Enforcement · United States · 2017-06-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2741-2017
Date of alert
2017-06-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Mako Surgical Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
05212015
Reported risk: An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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