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Perifix® 332086 (UDI 04046964177323)Recalls & reported problems

B. Braun Medical Inc. · PERIFIX® 17 Ga. x 3-1/2 in. (90 mm) Tuohy, PERIFIX FX 19 Ga. Springwound Open Tip Catheter, 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 04046964177323), received between May 2, 2019 and May 2, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component2

Patient problems

  • No Known Impact Or Consequence To Patient2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 2, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

    AS PER USER FACILITY, EVENT 1: CATHETER CONNECTORS ARE DETACHING FROM THE CATHETER. THEY ARE NOT TAPING THE CATHETER CONNECTOR. THEY CUT AND CLEANSED CATHETERS AND ADDED A NEW CONNECTOR. A SPECIFIC NUMBER OF OCCURRENCES WAS NOT PROVIDED. NO PATIENT INJURY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8574853 ↗
  • MalfunctionMay 2, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

    AS PER USER FACILITY, EVENT 2: CATHETER CONNECTORS ARE DETACHING FROM THE CATHETER. THEY ARE NOT TAPING THE CATHETER CONNECTOR. THEY CUT AND CLEANSED CATHETERS AND ADDED A NEW CONNECTOR. A SPECIFIC NUMBER OF OCCURRENCES WAS NOT PROVIDED. NO PATIENT INJURY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8574852 ↗

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