SpO2 Masimo Cable LNCS 1.2m MS24303Recalls & reported problems
Draeger Medical Systems, Inc. · Class 2
Data updated Oct 16, 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 04049098003032), received between Sep 15, 2025 and Sep 15, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Connection 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Connection Problem1
- Material Integrity Problem1
- Protective Measures Problem1
- Therapeutic or Diagnostic Output Failure1
- Unable to Obtain 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 15, 2025Unable to Obtain Readings; Connection Problem; Material Integrity Problem; Protective Measures Problem; Therapeutic or Diagnostic Output Failure
WE WERE TRANSFERRING AN INTUBATED PT. ZOLL MONITOR SAID SENSOR FAILURE ON THE PULSE OX CABLE. WE CHANGED SENSORS AND WE TURNED MACHINE OFF AND THEN ON AGAIN. AFTER FIDDLING WITH IT SEVERAL MINUTES, IT WAS DETERMINED THE CABLE WAS THE PROBLEM. WE COULD NOT MONITOR O2 SATURATION DURING FLIGHT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23051344 ↗
Other Cable, Transducer And Electrode, Patient, (Including Connector) devices
- IntraSight 797403Philips Image Guided Therapy Corporation · Cable, Transducer And Electrode, Patient, (Including Connector)82 reports
- ASSY, CABLE, ECG, 15 LEAD, 3 WIRE PRECOR 11111Physio-Control, Inc. · CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR)1 recall0 reports
- MR Patient Care Short Wide ECG 2.0 Cable AAMI CAB,4 LD,CV MRI ECGPhilips Ds North America LLC · CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR)12 reports
- NA 5492VLMedtronic, Inc. · CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR)10 reports
- NA 5492ALMedtronic, Inc. · CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR)10 reports
- NA 5487LMedtronic, Inc. · CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR)8 reports
- CORE M2 Vascular System 400-0100.17Volcano Corporation · Cable, Transducer And Electrode, Patient, (Including Connector)6 reports
- NA 5487Medtronic, Inc. · CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR)6 reports
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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