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Design Options® 552177Recalls & reported problems

B. Braun Medical Inc. · CESK UNIVERSITY OF ILLINOIS MED CTR · Class 2

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

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

2 FDA recall records name this device's identifier, 2 still open.

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.

Recalls naming this device

  1. Sep 18, 2025Open, Classified

    Potential for the lid of the catheter connector to be in the incorrect position.

    Z-0126-2026 · Root cause: Process control · FDA record ↗

  2. Jun 5, 2023Open, Classified

    Kits were assembled with the incorrect Filter Straw.

    Z-2003-2023 · Root cause: Mixed-up of materials/components · FDA record ↗

Other Epidural anesthesia kit devices

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