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Design Options® 555215Recalls & reported problems

B. Braun Medical Inc. · Continuous Epidural Tray · Class 2

All models of Design Options (116)

Data updated Oct 16, 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 04046964314452), received between Aug 6, 2019 and Aug 6, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

  • MalfunctionAug 6, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

    AS REPORTED BY THE USER FACILITY: CUSTOMER REPORTS THAT THE CATHETER CONNECTOR DISCONNECTED. NO INJURY REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8863812 ↗
  • MalfunctionAug 6, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

    AS REPORTED BY THE USER FACILITY: CUSTOMER REPORTS A CATHETER MISCONNECTION ISSUE. LIMITED INFORMATION PROVIDED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8863808 ↗

Other Epidural anesthesia kit devices

All Epidural anesthesia kit devices →

Sources and updates

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