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Design Options® 555779Recalls & 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
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 04046964316944), received between Jul 11, 2019 and Jul 11, 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.

  • MalfunctionJul 11, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

    AS REPORTED BY THE USER FACILITY: CUSTOMER REPORTS THAT THE CATHETER CONNECTORS ARE DISCONNECTING. NO INJURY REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8781007 ↗
  • MalfunctionJul 11, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

    AS REPORTED BY THE USER FACILITY: CUSTOMER REPORTS THAT THE CATHETER CONNECTORS ARE DISCONNECTING. NO INJURY REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8781005 ↗

Other Epidural anesthesia kit devices

All Epidural anesthesia kit devices →

Sources and updates

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