Medex MX252LRecalls & reported problems
Icu Medical, Inc. · Class 2
All models of Medex (98)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10351688508232), received between Mar 21, 2023 and Mar 10, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (2 reports).
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
- Loose or Intermittent Connection2
- Connection Problem1
- Fluid/Blood Leak1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 10, 2025Loose or Intermittent Connection; Loose or Intermittent Connection
IT WAS REPORTED THAT THE STOP COCK CAME OFF THE END OF THE IV TUBING. THE PRODUCT FAULT OCCURRED DURING INFUSION WHILE IN USE WITH A PATIENT. THE TUBING WAS CHANGED OUT. THERE WAS PATIENT INVOLVEMENT, AND NO PATIENT HARM/ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21560612 ↗MalfunctionApr 21, 2023Loose or Intermittent Connection; Loose or Intermittent Connection
IT WAS REPORTED THAT THE CONNECTION WAS FOUND LOOSE BETWEEN THE STOPCOCK AND INTRAVENOUS (IV).THE IV WAS REMOVED AND SECONDARY IV STARTED IN OTHER EXTREMITY USING THE SAME EQUIPMENT. MAGNETIC RESONANCE IMAGING (MRI) STAFF REPORTED THAT A SIMILAR EVENT OCCURRED FROM THE FIRST SCAN. THE CONNECTION CAME LOOSE, CAUSING LOSS OF MEDICATION AND LOSS OF IV ACCESS. NO PATIENT INJURY WAS REPORTED..
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16787487 ↗MalfunctionMar 21, 2023Fluid/Blood Leak; Connection Problem; Fluid/Blood Leak; Connection Problem
IT WAS REPORTED THAT THE DEVICE CONNECTION CAME LOOSE CAUSING LOSS OF MEDICATION AND LOSS OF IV ACCESS. NO MEDICAL OR SURGICAL INTERVENTION WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16580297 ↗
Other Stopcock, i.V. Set devices
- Connecta, Luer-Lok 394910BD Switzerland Sàrl · Stopcock, i.V. Set3 recalls8 reports
- Outlook® 490361B. Braun Medical Inc. · Stopcock, i.V. Set3 recalls0 reports
- Blood Administration Set 490530B. Braun Medical Inc. · Stopcock, i.V. Set2 recalls11 reports
- Medex MX9341LIcu Medical, Inc. · Stopcock, i.V. Set63 reports
- ICU Medical AC135Icu Medical, Inc. · Stopcock, i.V. Set1 recall10 reports
- IV Administration Set 490067B. Braun Medical Inc. · Stopcock, i.V. Set1 recall9 reports
- ICU Medical MC330174Icu Medical, Inc. · Stopcock, i.V. Set1 recall4 reports
- IV Administration Set 490432B. Braun Medical Inc. · Stopcock, i.V. Set1 recall3 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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