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N/A 403250Recalls & reported problems

Becton, Dickinson And Company · ADAPTER CATHETER S/SU · 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 00382904032500), received between Dec 7, 2020 and Dec 7, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Leak/Splash” (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

  • Leak/Splash1

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.

  • MalfunctionDec 7, 2020Leak/Splash; Leak/Splash

    IT WAS REPORTED THAT ADAPTER CATHETER S/SU LEAKED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO.: 403250, BATCH NO.: 9352479. IT WAS REPORTED THAT THE DYE IS COMING OUT OF THE SIDE WHEN THE CATHETER IS INSERTED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10962225 ↗

Other Anesthesia conduction kit devices

All Anesthesia conduction kit devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.