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Discofix® 455991Recalls & reported problems

B. Braun Medical Inc. · Three-way stopcock with luer slip · Class 1

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 04046964996986), received between Jan 16, 2020 and Jan 16, 2020 — 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 Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 16, 2020Fluid/Blood Leak; Fluid/Blood Leak

    AS REPORTED BY THE USER FACILITY: IT WAS REPORTED THAT DURING USE OF THE PRODUCT BLOOD WAS COMING OUT. NO INJURY REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9595924 ↗

Other ACCESSORIES, CATHETER devices

All ACCESSORIES, CATHETER devices →

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