B Braun recalls spinal epidural anesthesia trays with potential for incorrect catheter connector lid position. Affected units include specific model and lot numbers. Contact for remedy details.
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun is recalling spinal and epidural anesthesia trays that may have a catheter connector lid in the wrong position. This could lead to improper use during medical procedures. Affected units have specific model numbers and lot dates.
The catheter connector lid might be in the wrong position, which could cause improper use during medical procedures. This might lead to incorrect placement of needles or catheters. However, the risk is not described as causing serious injury in normal use.
Healthcare professionals using the recalled spinal and epidural anesthesia trays are most at risk. Patients receiving procedures with these trays may be affected if the lid position is incorrect.
Check for the product code NES1727KFX on the tray. Look for lot numbers 0062000732 or 0062012053. The expiration date is July 31, 2026.
Look for the product code NES1727KFX, lot numbers 0062000732 or 0062012053, and expiration date July 31, 2026.
The recall states there is a potential for the lid to be in the incorrect position, but it does not specify that this causes serious injury in normal use. The product may be safe for most uses.
The recall does not provide a remedy, so no action is required unless the lid position is incorrect. Check the product details to confirm if it is affected.
Check for the product code NES1727KFX, lot numbers 0062000732 or 0062012053, and expiration date July 31, 2026.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0123-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0123-2026 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.
