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Multi-Link 2017006-001Recalls & reported problems

Carefusion Finland 320 Oy · ECG Care Cable 12-Lead, AHA, 3.6 m/12 ft · 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 10885403255991), received between Sep 1, 2021 and Sep 1, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (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.

Most reported problems

Device problems

  • Incorrect, Inadequate or Imprecise Result or Readings1

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.

  • MalfunctionSep 1, 2021Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

    THE CUSTOMER REPORTED THAT THE ECG MACHINE WAS ALARMING AN ASYSTOLE CONTINUOUSLY EVEN AFTER THE 2017006-001 MULTI-LINK¿ ECG CARE CABLE, 12-LEAD, AHA, 3.6M / 12 FT CABLES ARE UNPLUGGED. THIS DEVICE IS DESIGNED FOR MONITORING AND DOES NOT PROVIDE MEDICATION. BASED ON THE AVAILABLE INFORMATION, THE CUSTOMER DID NOT REPORT ANY PATIENT OR USER HARM AS A RESULT OF THE ISSUE DESCRIBED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12409717 ↗

Other CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR) devices

All CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.