Design OptionsRecalls & reported problems across all models
B. Braun Medical Inc. · 116 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Design Options models — page 2
116 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Design Options® 530192Spinal epidural anesthesia kit1 report
- Design Options® 551148Epidural anesthesia kit1 report
- Design Options® 551366Epidural anesthesia kit1 report
- Design Options® 530112Spinal epidural anesthesia kit1 report
- Design Options® 530142Epidural anesthesia kit1 report
- Design Options® 551344Epidural anesthesia kit1 report
- Design Options® 551771Epidural anesthesia kit1 report
- Design Options® 551942Epidural anesthesia kit1 report
- Design Options® 551951Epidural anesthesia kit1 report
- Design Options® 552030Epidural anesthesia kit1 report
- Design Options® 552038Epidural anesthesia kit1 report
- Design Options® 555070Epidural anesthesia kit1 report
- Design Options® 555170Epidural anesthesia kit1 report
- Design Options® 555449Epidural anesthesia kit1 report
- Design Options® 552083Epidural anesthesia kit1 report
- Design Options® 530164Spinal epidural anesthesia kit1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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