MaxGuard, MaxPlus MP9233-CRecalls & reported problems
BD Switzerland Sàrl · Tri-fuse extension set, (minibore) 3 clear needleless connector 18 cm (7 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 10885403237089), received between Feb 27, 2019 and Feb 27, 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
- Fracture1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 27, 2019Fluid/Blood Leak; Fracture; Fluid/Blood Leak; Fracture
THE CUSTOMER REPORTED ONE OF THE NEEDLELESS CONNECTORS ON A MAXPLUS TRIFUSE CRACKED AND LEAKED DURING PATIENT USE. THE CUSTOMER WOULD LIKE TO KNOW IF THE CRACK ORIGINATED FROM THE INSIDE OR THE OUTSIDE OF THE PRODUCT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8376258 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.