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Perifix® 332224Recalls & reported problems

B. Braun Medical Inc. · PERIFIX® 17 Ga. x 3-1/2 in. (90 mm) Tuohy, PERIFIX 20 Ga. Closed Tip Catheter, 5 mL Glass Luer Lock LOR Tray (Kit) · Class 2

Data updated Oct 13, 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 04046964178405), received between Nov 28, 2016 and Nov 28, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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

  • Device Operates Differently Than Expected1

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.

  • MalfunctionNov 28, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected

    AS REPORTED BY THE USER FACILITY: REPORTS THE EPIDURAL CATHETER BROKE AT THE POINT OF THE MOST DISTAL TAPING TO THE PATIENT'S BACK. A SECOND CATHETER WAS THEN PLACED IN THE PATIENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 6128831 ↗

Other Epidural anesthesia kit devices

All Epidural anesthesia kit devices →

Sources and updates

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