MaxZero MZ9274Recalls & reported problems
BD Switzerland Sàrl · Microbore tri fuse extension set, 3 IV connectors, 2 filters, 15 cm (6 in) · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885403240751), received between May 15, 2025 and May 15, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Free or Unrestricted Flow” (2 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.
Reports received per month
Most reported problems
Device problems
- Free or Unrestricted Flow2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 15, 2025Free or Unrestricted Flow; Free or Unrestricted Flow
IT WAS REPORTED THAT BD MAZZERO EXTENSION SET HAD AIR IN LINE THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE FOLLOWING VERBATIM IT WAS REPORTED BY CUSTOMER THAT THE J LOOPS FILLED WITH AIR WHILE ATTEMPTING TO DRAW LABS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22028829 ↗MalfunctionMay 15, 2025Free or Unrestricted Flow; Free or Unrestricted Flow
IT WAS REPORTED THAT BD MAZZERO EXTENSION SET HAD AIR IN LINE THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE FOLLOWING VERBATIM IT WAS REPORTED BY CUSTOMER THAT THE J LOOPS FILLED WITH AIR WHILE ATTEMPTING TO DRAW LABS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22028827 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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