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Design Options® 551771Recalls & reported problems

B. Braun Medical Inc. · Continuous Epidural Tray · 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 04046964308048), received between Dec 27, 2021 and Dec 27, 2021 — 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. How this data works · Data updated Oct 13, 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.

  • MalfunctionDec 27, 2021Break; Break

    AS REPORTED BY THE USER FACILITY: IT WAS REPORTED THAT DURING THE CATHETER WITHDRAWAL, THE BLUE TIP WAS MISSING.

    Patient problems: Foreign Body In Patient

    MAUDE report 13090731 ↗

Other Epidural anesthesia kit devices

All Epidural anesthesia kit devices →

Sources and updates

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