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Perifix® 332095Recalls & reported problems

B. Braun Medical Inc. · CE17TKFSDTD EPID TRAY W/17GA FIXED WING · Class 2

All models of Perifix (57)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 04046964954276), received between Jun 17, 2021 and Jun 17, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Break1
  • Fluid/Blood Leak1

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.

  • MalfunctionJun 17, 2021Break; Fluid/Blood Leak; Break; Fluid/Blood Leak

    AS REPORTED BY THE USER FACILITY: FX EPIDURAL CATHETER POSSIBLE SHEARING. ON JUNE 5TH, THE DOCTOR BELIEVES HE HAD CATHETER SHEARING, BUT NOTHING WAS FOUND ON SCAN OF PATIENT. DURING THE PROCEDURE, THE DOCTOR FELT NO RESISTANCE, SO HE REMOVED THE CATHETER. NO INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12018309 ↗

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Sources and updates

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