B Braun Medical Inc 2026-06-10 Health critical FDA
Health · FDA · Recall #FDA-Z-2277-2026
Spinocan Spinal Needle procedure kits: Material Description (Material Number): … Recall
Issued June 10, 2026 · B Braun Medical Inc
In June 2026, B Braun Medical Inc recalled the Spinocan Spinal Needle procedure kits: Material Description (Material Number): …, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
What you should do
- 1 Stop using Spinocan Spinal Needle procedure kits: Material Description (Material Number): … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact B Braun Medical Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- B Braun Medical Inc
- Category
- Health
- Recall date
- June 10, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-2277-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- B Braun Medical Inc has 23 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.