B Braun recalls ESPOCAN spinal/epidural anesthesia trays due to potential incorrect catheter connector lid position. Affected units have specific product codes and lot numbers. Consumers should contact for details.
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun is recalling ESPOCAN spinal and epidural anesthesia trays and needles because the lid of the catheter connector might be in the wrong position. This could lead to improper use during medical procedures. If you own the recalled items, contact B Braun for instructions.
The catheter connector lid might be in the incorrect position, which could lead to improper use during medical procedures. This might cause the equipment to function incorrectly, potentially affecting the safety of the procedure.
Healthcare professionals using the ESPOCAN anesthesia trays and needles for spinal or epidural procedures are most at risk. Patients receiving these procedures may also be affected if the equipment is used incorrectly.
Check for product code ES1725KFX on the ESPOCAN Combined Spinal and Epidural Anesthesia Tray. Lot numbers 0062005817, 0062011662, 0062011663, 0062014354, and 0062011664 are affected. The expiration date is July 31, 2026.
Look for product code ES1725KFX and affected lot numbers on the ESPOCAN anesthesia tray.
The recall states there is a potential for the lid to be in the incorrect position, which could lead to improper use during procedures. However, the hazard is not described as causing serious injury in normal use.
Check for product code ES1725KFX and lot numbers 0062005817, 0062011662, 0062011663, 0062014354, or 0062011664 on the ESPOCAN anesthesia tray.
The recall does not specify a remedy; contact B Braun directly for 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-0122-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0122-2026 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.
