BD MaxPlus MPX9101-CRecalls & reported problems
BD Switzerland Sàrl · Extension set, (minibore) with clear needleless connector and Y-site 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 10885403237270), received between Jan 6, 2023 and Jan 6, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Separation” (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
- Material Separation1
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.
MalfunctionJan 6, 2023Material Separation; Material Separation
IT WAS REPORTED THAT THE BD MAXPLUS¿ EXTENSION SET WITH NEEDLELESS CONNECTOR AND Y-SITE DISCONNECTED AT THE CONNECTION POINT DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "SIN 82991 MPX9101-C EXTENSION SET FOUND DISCONNECTED AT POINT NOT FOR CONNECTION. NO INCIDENT OF TUGGING, PULLING OR CATCHING ON ANYTHING IDENTIFIED. PATIENT NOT CLINICALLY ABLE TO BREAK/DISCONNECT LINE AT POINT OF DISCONNECTION.."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16118388 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.