Design Options® 530201Recalls & reported problems
B. Braun Medical Inc. · NES1725KFXL SPINAL EPID CLOSED TIP CATH · Class 2
All models of Design Options (116)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Jan 29, 2026Open, Classified
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
Z-2265-2026 · Root cause: Process control · Recall details · FDA record ↗
Other Spinal epidural anesthesia kit devices
- Medline Industries, Inc. DYNJRA9040Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls2 reports
- Design Options® 530184B. Braun Medical Inc. · Spinal epidural anesthesia kit2 recalls1 report
- Medline Industries, Inc. DYNJ34418MMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls1 report
- Medline Industries, Inc. DYNJRA2013Medline 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. DYNJRA1869Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1979AMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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