BD MaxPlus MP9229Recalls & reported problems
BD Switzerland Sàrl · Extension Set, (minibore) with Needleless Connector 36 cm (14 in) · Class 2
All models of BD MaxPlus (9)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10885403237058), received between Sep 25, 2019 and Sep 26, 2019 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Material Separation” (4 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.
Most reported problems
Device problems
- Material Separation4
Patient problems
- No Information4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 26, 2019Material Separation; Material Separation
IT WAS REPORTED THAT EXTENSION SETS CAME APART. LAST WEEK WE HAD THE SAME PROBLEM, THE 14' EXTENSION SET WAS SHOOTING OFF THE SYRINGES.
Patient problems: No Information
MAUDE report 9123289 ↗MalfunctionSep 26, 2019Material Separation; Material Separation
IT WAS REPORTED THAT EXTENSION SETS CAME APART. THE CUSTOMER STATED THAT THE 7" SETS BROKE APART WHILE BEING USED BY A DIFFERENT NURSE WHILE IN THE FIELD SEEING A PATIENT.
Patient problems: No Information
MAUDE report 9123286 ↗MalfunctionSep 25, 2019Material Separation; Material Separation
IT WAS REPORTED THAT EXTENSION SETS CAME APART. THE FUSED END SHOT ACROSS THE ROOM WHILE BEING USED IN THE INFUSION SUITES. NOBODY WAS HURT BUT THEY WERE CONCERNED ABOUT THIS HAPPENING.
Patient problems: No Information
MAUDE report 9120863 ↗MalfunctionSep 25, 2019Material Separation; Material Separation
IT WAS REPORTED THAT EXTENSION SETS CAME APART. THE FUSED END SHOT ACROSS THE ROOM WHILE BEING USED IN THE INFUSION SUITES. NOBODY WAS HURT BUT THEY WERE CONCERNED ABOUT THIS HAPPENING.
Patient problems: No Information
MAUDE report 9120861 ↗
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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 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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