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Perifix® 332249Recalls & reported problems

B. Braun Medical Inc. · PERIFIX® 18 Ga. x 3-1/2 in. (90 mm) Hustead, 5 mL Glass Luer Lock LOR Tray (Kit) · Class 2

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 04046964178702), received between Mar 24, 2022 and Mar 24, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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.

Most reported problems

Device problems

  • Contamination /Decontamination Problem2

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.

  • MalfunctionMar 24, 2022Contamination /Decontamination Problem; Contamination /Decontamination Problem

    AS REPORTED BY THE USER FACILITY: EVENT 1: IT WAS REPORTED THE CLINICIANS FOUND MOISTURE IN GLASS LL SYRINGE. NO INJURIES WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13894264 ↗
  • MalfunctionMar 24, 2022Contamination /Decontamination Problem; Contamination /Decontamination Problem

    AS REPORTED BY THE USER FACILITY: EVENT 2. IT WAS REPORTED THE CLINICIANS FOUND MOISTURE IN GLASS LL SYRINGE. NO INJURIES WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13894223 ↗

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