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CONTIPLEX® 332103Recalls & reported problems

B. Braun Medical Inc. · Contiplex® Nerve Block Support Tray (Kit) with Ultrasound Transducer Cover and Gel (NB400) · Class 2

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 04046964177422), received between May 15, 2019 and May 15, 2019 — classified as 1 malfunction.

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

  • Contamination /Decontamination Problem1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionMay 15, 2019Contamination /Decontamination Problem; Contamination /Decontamination Problem

    AS REPORTED BY THE USER FACILITY: THE CUSTOMER OPENED A TRAY AND DISCOVERED FLUID DROPLETS WITHIN THE SYRINGE. NO INJURY REPORTED.

    Patient problems: No Patient Involvement

    MAUDE report 8612047 ↗

Other Nerve block tray devices

All Nerve block tray devices →

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