REAL INTELLIGENCE ROB100021Recalls & reported problems
Smith & Nephew, Inc. · REAL INTELLIGENCE ROBOTICS CART BASE 120 · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556774144), received between Apr 9, 2024 and Apr 9, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Battery Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Battery Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 9, 2024Battery Problem; Battery Problem
IT WAS REPORTED THAT DURING A CORI-ASSISTED TKA, CORI SHUT OFF COMPLETELY WITH NO POWER. THERE WAS NO BLUE MAN WITH MANUAL, JUST BLACK. UNPLUGGED AND REPLUGGED EVERY PLUG ON THE CORI UNIT AND THE TRANSFORMER BOX AND TRIED SIX DIFFERENT OUTLETS IN THE ROOM. THERE WAS STILL NO POWER TO THE UNIT. THEY THINK IT IS A SHORT IN THE FUSE INSIDE OF THIS BOX. SURGERY WAS PERFORMED, WITHOUT ANY DELAY, CHANGING TO MANUAL PROCEDURE. NO PATIENT COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19076032 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.