Multi-Link 416467-001Recalls & reported problems
Carefusion Finland 320 Oy · ECG Leadwire V-lead, Grabber, AHA, 130 cm/51 in · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403257162), received between Aug 22, 2022 and Aug 22, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Defective Component” (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
- Defective Component1
Patient problems
- Cardiac Arrest1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 22, 2022Defective Component; Defective Component
IT WAS REPORTED TO VYAIRE MEDICAL THAT WHILE A PATIENT WAS CODING THE LEADWIRE MULTILINK V-LEAD GRAB AHA SET L WAS GETTING SEVERAL LEADS FAIL ON THE PATIENT. THE EKG MONITOR IS NOT PICKING UP THE EKG. CLIENTS CHANGED OUT THE PDM, 12 LEADS, AND ELECTRODES AFTER THE INITIAL FAILURE. A SECOND SET OF LEADS STILL SHOWED RL LEAD FAIL. THEY WOULD GET AN EKG, BUT BEFORE SENDING 12 LEAD EKG THE VITALS WOULD DISAPPEAR. THE LEADS WERE REPLACED FOR THE THIRD TIME AND THE FAILURE WAS RESOLVED. THE NURSES DID NOT REPORT PATIENT HARM. HOWEVER, FAILURE TO GET AN EKG ON A CODING PATIENT WAS A DELAY IN PATIENT CARE DURING A CARDIAC ARREST.
Patient problems: Cardiac Arrest
MAUDE report 15272499 ↗
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- NA 5492VLMedtronic, Inc. · CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR)10 reports
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- CORE M2 Vascular System 400-0100.17Volcano Corporation · Cable, Transducer And Electrode, Patient, (Including Connector)6 reports
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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