B Braun recalls Combined Spinal and Epidural Anesthesia Tray 2 with potential for incorrect catheter connector lid position. Affected units include specific model and lot numbers. Contact for remedy.
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun is recalling a specific anesthesia tray and needles due to a risk that the catheter connector lid might be in the wrong position. This could lead to improper use during medical procedures, though the recall does not specify serious injury risks.
The catheter connector lid might be in the incorrect position, which could lead to improper needle placement during anesthesia procedures. This may cause complications if the equipment is not correctly set up for the procedure.
Healthcare professionals using the recalled tray and needles for spinal or epidural anesthesia procedures. Patients receiving these procedures are at risk if the equipment is used without proper configuration.
Check for the product code SESK on the tray. The specific model includes PERIFIX 17 Ga. x 3-1/2 in. Tuohy Epidural Needle and PENCAN 27 Ga. x 5 in. Spinal Needle. Units were sold with lot number 0062003227 and expire July 31, 2026.
Look for the product code SESK on the tray to confirm if it is affected.
The recall states a potential for the catheter connector lid to be in the incorrect position, but it does not specify serious injury risks or immediate danger.
Check for product code SESK on the tray. The specific model includes PERIFIX 17 Ga. x 3-1/2 in. Tuohy Epidural Needle and PENCAN 27 Ga. x 5 in. Spinal Needle with lot number 0062003227.
The recall does not specify a remedy, so contact B Braun for further instructions.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0125-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0125-2026 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.
