Braun Medical recalls spinal needle procedure kits containing Bupivacaine Hydrochloride due to potential quality issues identified during FDA facility inspections. Affected kits have specific material numbers and batch numbers.
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.
Braun Medical is recalling spinal needle procedure kits that contain Bupivacaine Hydrochloride because the manufacturer identified potential quality issues during an FDA inspection. These kits could pose risks if used improperly.
The recall is due to potential quality issues with the Bupivacaine Hydrochloride in the kits, which were identified during an FDA inspection. The exact nature of the quality issue is not specified in the recall notice.
Healthcare professionals and patients who use these spinal needle kits for medical procedures are most at risk. The recall affects specific product models with particular batch numbers.
Check for the material numbers 333867, 333862, 332607, 333868, 333865, 333871, or 333851 on the packaging. Also look for batch numbers listed in the recall notice.
Review the material number and batch numbers on the packaging to determine if your kit is affected.
The manufacturer identified potential quality issues with the Bupivacaine Hydrochloride in the kits during an FDA facility inspection.
The recall notice does not specify a remedy, so check the product details to see if it is affected and contact the manufacturer for further instructions.
Yes, specific batch numbers are listed in the recall notice for each material number, but the exact list is too long to summarize here.
We’ve drafted a message you can send Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2276-2026 — Braun Medical Braun Medical Hello, I own a Braun Medical that is covered by recall Z-2276-2026 from 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.
