FDA recall notice
Convenience Kit Recall: B. Braun Medical, Inc. Removes Spinal Anesthesia Kits Containing…
FDA Recall Confirmed · Spinal Anesthesia Kit · posted Jul 16, 2026
Key facts
| Notice | Convenience Kit Recall: B. Braun Medical, Inc. Removes Spinal Anesthesia Kits Containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP |
|---|---|
| Device type | Spinal Anesthesia Kit |
| Status | Recall Confirmed |
| Posted | Jul 16, 2026 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- 1–9 Recall events referenced
- None UDI device identifiers named
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recall notices and early alerts
The FDA's Medical Device Recalls and Early Alerts list covers the most serious device recalls, plus early alerts about potentially high-risk device issues while the FDA is still collecting information. A notice is updated as the recall is confirmed or changes.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls and Early Alerts · Source date: