BD MaxPlus MP9027-CRecalls & reported problems
BD Switzerland Sàrl · Bi-Fuse Extension Set, with 2 removable clear needleless connector 13 cm (5 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 10885403236907), received between Mar 28, 2019 and Mar 28, 2019 — 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
Patient problems
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 28, 2019Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THE BI-FUSE EXTENSION SET LEAKED DURING AN INFUSION. ALTHOUGH REQUESTED, NO FURTHER INFORMATION HAS BEEN RECEIVED.
Patient problems: No Information
MAUDE report 8462173 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.