Design Options® 530171Recalls & reported problems
B. Braun Medical Inc. · Combined Spinal/Epidural Tray · Class 2
1 open recall names 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
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 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
- Sep 18, 2025Open, Classified
Potential for the lid of the catheter connector to be in the incorrect position.
Z-0124-2026 · Root cause: Process control · FDA record ↗
Other Spinal epidural anesthesia kit devices
- Medline Industries, Inc. DYNJRA9040Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls2 reports
- Medline Industries, Inc. DYNJ34418MMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls1 report
- Design Options® 530184B. Braun Medical Inc. · Spinal epidural anesthesia kit2 recalls1 report
- Medline Industries, Inc. DYNJRA1849Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1739AMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1850Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1739BMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Design Options® 530159B. Braun Medical Inc. · Spinal epidural anesthesia kit2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.