BD MaxPlus MPX9102-CRecalls & reported problems
BD Switzerland Sàrl · Kink resistant extension set, with clear needleless connector and Y-site 24 cm (9.25 in) · Class 2
- Adverse event reports
- 22
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 22 adverse event reports that list this exact device (DI 10885403237287), received between Jun 14, 2019 and Jul 12, 2019 — classified as 22 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (22 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Fluid/Blood Leak22
Patient problems
- No Consequences Or Impact To Patient19
- No Information3
Recent adverse event reports
The 22 most recent of 22 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8786221 ↗MalfunctionJul 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8785954 ↗MalfunctionJul 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8785948 ↗MalfunctionJul 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8785883 ↗MalfunctionJul 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8785882 ↗MalfunctionJul 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8785879 ↗MalfunctionJul 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8785841 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782865 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782824 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782823 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782822 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782821 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782820 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782784 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782782 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782781 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782744 ↗MalfunctionJul 11, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE MAXPLUS EXTENSION SET LEAKED IN THE ER. THERE WAS NO HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8782742 ↗MalfunctionJun 21, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT BLOOD AND/OR LACTATED RINGERS LEAKED IN THE LAST COUPLE MONTHS.
Patient problems: No Information
MAUDE report 8724585 ↗MalfunctionJun 21, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT BLOOD AND/OR LACTACTED RINGERS LEAKED IN THE LAST COUPLE MONTHS.
Patient problems: No Information
MAUDE report 8724488 ↗MalfunctionJun 14, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT SET IS LEAKING AROUND END PIECE.
Patient problems: No Information
MAUDE report 8698632 ↗MalfunctionJun 14, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE SET LEAKED LACTATED RINGERS AT THE CONNECTION SITE DURING PATIENT USE. THE PATIENT'S IV REMAINED IN PLACE, AND THE EXTENSION SET WAS REPLACED. THERE WAS NO PATIENT HARM REPORTED AS A RESULT OF THIS EVENT..
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8698568 ↗
Other Set, administration, intravascular devices
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- Autosoft90™ 1002817Unomedical A/S · Set, Administration, Intravascular1 recall11,907 reports
- Minimed™ Quick-set™ MMT-399AUnomedical A/S · Set, Administration, Intravascular9 deaths8,669 reports
- Medtronic Extended MMT-431AUnomedical A/S · Set, Administration, Intravascular3 deaths8,574 reports
- MiniMed™ Mio™ Advance MMT-242AUnomedical A/S · Set, Administration, Intravascular15 deaths8,164 reports
- CADD 21-7302-24Icu Medical, Inc. · Set, administration, intravascular4 recalls1 death4,657 reports
- Autosoft XC 1001681Unomedical A/S · Set, Administration, Intravascular1 death4,216 reports
- Minimed™ Quick-set™ MMT-397AUnomedical A/S · Set, Administration, Intravascular19 deaths4,134 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.