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IntelliCart™ UE514010400Recalls & reported problems

Zimmer Orthopaedic Surgical Products, Inc. · Class 2

All models of IntelliCart (8)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 00889024501652), received between Feb 22, 2022 and Feb 22, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Frayed” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Material Frayed1

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.

  • MalfunctionFeb 22, 2022Material Frayed; Material Frayed

    IT WAS REPORTED THAT DURING SITE INSPECTION THE WYE POWER CORD OF THE PRODUCT HAD BEEN DAMAGED AND HAD EXPOSED WIRES NEAR THE WALL PLUG. NO ADVERSE EVENTS WERE REPORTED AS A RESULT OF THIS MALFUNCTION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13579795 ↗

Other APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED devices

All APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED devices →

Sources and updates

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