BD MaxPlus MP9081-CRecalls & reported problems
BD Switzerland Sàrl · Kink resistant extension set, with clear needleless connector 20 cm (8 in) · Class 2
- 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 10885403236914), received between Jul 8, 2021 and Jul 8, 2021 — 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Fluid/Blood Leak1
- Material Rupture1
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.
MalfunctionJul 8, 2021Fluid/Blood Leak; Material Rupture; Fluid/Blood Leak; Material Rupture
IT WAS REPORTED THAT THE 8 IN KINK RESISTANT SET W/MAXPLUS EXPERIENCED RUPTURED TUBING. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: SALES REP HAS A CUSTOMER THAT INFORMED HIM THAT THE MAXPLUS EXTENSION SET MP9081-C IS BURSTING AROUND 250 PSI. SAYS PACKAGING SAYS BURST RATE IS AROUND 325 PSI.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12136924 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.