FDA Device Intelligence
HomeB. BRAUN MEDICAL INC. › Spinocan®

Spinocan®

B. BRAUN MEDICAL INC. · Model 333231 · UDI-DI 04046964179488

OFU Prescription
0
510(k) clearances
146
Adverse events
3
Recalls
16
Facilities

Description

Spinocan® 22 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit)

Recalls

DateFirmReason
2026-05-06B Braun Medical IncThese procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti
2026-05-06B Braun Medical IncThese procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti
2026-05-06B Braun Medical IncThese procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.