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Perifix® 332292Recalls & reported problems

B. Braun Medical Inc. · PERIFIX® 20 Ga. x 2 in. (50 mm) Tuohy, PERIFIX ONE 24 Ga. Closed Tip Catheter, 5 mL Glass Luer Slip LOR Tray (Kit) - Pediatric Tray · 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 04046964179044), received between Feb 20, 2020 and Feb 20, 2020 — 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

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • MalfunctionFeb 20, 2020Break; Break

    AS REPORTED BY THE USER FACILITY: THERE WAS RESISTANCE MET WHEN THREADING THE CATHETER. UPON REMOVAL OF THE CATHETER, IT WAS NOTED THAT THE TIP WAS MISSING. NO ADDITIONAL INFORMATION PROVIDED.

    Patient problems: Foreign Body In Patient

    MAUDE report 9731956 ↗

Other Epidural anesthesia kit devices

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Sources and updates

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