B Braun Medical recalls certain spinal needle anesthesia procedure kits due to potential quality issues identified during FDA inspection. Affected kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP.
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
B Braun Medical is recalling specific spinal needle anesthesia procedure kits that contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to potential quality issues found during an FDA inspection of the manufacturer's facility.
The recall is based on potential quality issues identified during a recent FDA manufacturing facility inspection. The manufacturer, Huons Co, Ltd., issued a voluntary recall of the Bupivacaine Hydrochloride in Dextrose Injection, USP.
Healthcare professionals and patients who use these spinal needle kits for anesthesia procedures are affected. The risk is primarily for those using the recalled kits in medical settings.
Check for the material numbers listed in the recall notice (e.g., SSK H M C, SSK S C H, etc.) and batch numbers (e.g., 0061960383, 0061972565). The kits were sold with specific UDI-DI codes and batch numbers as detailed in the recall notice.
Review the material numbers and batch numbers listed in the recall notice to determine if your kit is affected.
The manufacturer, Huons Co, Ltd., issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
Check the material numbers and batch numbers listed in the recall notice to determine if your kit is affected. If it is, contact B Braun Medical for further instructions.
The recall is based on potential quality issues identified during an FDA inspection, but the specific risk is not detailed in the official notice.
We’ve drafted a message you can send B Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2278-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-2278-2026 from B Braun Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
