B Braun recalls PERIFIX FX Epidural Anesthesia Trays (Product Code CESK) due to potential incorrect catheter connector lid position. Affected units sold at hospitals from 2006-2026.
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun is recalling PERIFIX FX Epidural Anesthesia Trays with Product Code CESK because the lid of the catheter connector might be in the wrong position. This could lead to improper use during medical procedures if not corrected.
The catheter connector lid might be in the incorrect position, which could lead to improper use during epidural anesthesia procedures. This might cause the connector to not function correctly, potentially affecting the procedure's safety and effectiveness.
Healthcare professionals and hospitals that purchased the PERIFIX FX Epidural Anesthesia Trays with Product Code CESK between 2006 and 2026. Patients receiving epidural anesthesia using these trays are at risk if the lid position is incorrect.
Check for Product Code CESK on the tray. The recall includes units sold at hospitals from 2006 to 2026 with specific lot numbers listed in the recall notice.
Look for Product Code CESK on the tray to confirm if it's affected.
The recall states there's a potential for the lid to be in the incorrect position, which could affect proper use during epidural procedures. However, the hazard is not described as causing serious injury in normal use.
Check for Product Code CESK on the tray. The recall includes units sold at hospitals from 2006 to 2026 with specific lot numbers listed in the notice.
The recall does not specify a remedy, so no action is required beyond checking if your product has the Product Code CESK.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0126-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0126-2026 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.
