B Braun recalls Spinocan spinal needle kits with potential quality issues found during FDA inspection. Affected kits include specific sizes and batch numbers. Consumers should check their product details and contact the manufacturer.
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 is recalling certain Spinocan spinal needle procedure kits due to potential quality issues identified during an FDA inspection. These kits contain Bupivacaine Hydrochloride in Dextrose Injection, which may pose risks if the product is not manufactured correctly.
The recall is due to potential quality issues identified during a recent FDA manufacturing facility inspection. The Bupivacaine Hydrochloride in Dextrose Injection could be affected by manufacturing defects, though the specific risks are not detailed in the notice.
Healthcare professionals using the recalled Spinocan spinal needle kits are most at risk. Patients receiving procedures with these kits may also be affected if the product is not properly manufactured.
Check for the product model numbers: Spinocan 26 Ga. x 3-1/2 in. (90 mm), Spinocan 25 Ga. x 3-1/2 in. (90 mm), or Spinocan 22 Ga. x 3-1/2 in. (90 mm). Look for batch numbers like 0061976152 or similar.
Identify the model number and batch number on the kit to confirm if it is affected.
The manufacturer, Huons Co, Ltd., issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
Spinocan Spinal Needle procedure kits with model numbers 333201, 333211, or 333231 and specific batch numbers.
Check the model number and batch number on the kit. Affected kits include specific sizes and batch numbers listed in the recall notice.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2277-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-2277-2026 from B Braun. 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.
