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Combined Spinal & Epidural 339115Recalls & reported problems

B. Braun Medical Inc. · NES1827KN SPINAL/EPIDURAL TRAY NRFIT · Class 2

All models of Combined Spinal & Epidural (3)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

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 18, 2026.

Recalls naming this device

  1. Jul 10, 2019Class IITerminated

    The filter capacity is not achieved due to damage of the filter membrane.

    Z-2467-2019 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Epidural anesthesia kit devices

All Epidural anesthesia kit devices →

Sources and updates

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