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Meritrans DTXPlus® 10884450619282Recalls & reported problems

Argon Critical Care Systems Singapore Pte. Ltd. · 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 10884450619282), received between May 17, 2023 and May 17, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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.

Most reported problems

Device problems

  • Fluid/Blood Leak1

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.

  • MalfunctionMay 17, 2023Fluid/Blood Leak; Fluid/Blood Leak

    THE ACCOUNT ALLEGES THAT DURING ART-LINE MONITORING OF A PATIENT, THE CONNECTION WAS LEAKING FLUID. THE CLINICAL STAFF NOTED A CRACK IN THE TUBING AT THE TRANSDUCER CONNECTION. THE DEVICE WAS REPLACED TO COMPLETE THE PROCEDURE FOR THE PATIENT. NO ADDITIONAL PATIENT CONSEQUENCES TO REPORT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16946570 ↗

Other System, measurement, blood-pressure, non-invasive devices

All System, measurement, blood-pressure, non-invasive devices →

Sources and updates

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