B Braun recalls PERIFIX FX epidural anesthesia trays due to potential incorrect lid position on catheter connectors. Affected units may need inspection and correction to prevent improper use during procedures.
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun is recalling certain PERIFIX FX epidural anesthesia trays 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 lid of the catheter connector might be in the incorrect position, which could lead to improper use during epidural anesthesia procedures. This might cause the catheter to not function correctly, potentially affecting the procedure's safety and effectiveness.
Healthcare professionals using the PERIFIX FX epidural anesthesia trays for procedures are most at risk. Patients receiving epidural anesthesia through these trays may be affected if the lid position is incorrect.
Check for the product code CE17TKFSDT on the tray. The product was sold with expiration date 07/31/2026 and lot number 0062003112.
Inspect the catheter connector lid to ensure it is in the correct position as per the manufacturer's instructions.
The recall indicates a potential issue with the lid position, so it is recommended to check the lid position before use to ensure it is correct.
The official recall does not specify a remedy for incorrect lid position; users should check the lid position and ensure it is correct before use.
Look for the product code CE17TKFSDT on the tray, which was sold with expiration date 07/31/2026 and lot number 0062003112.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0118-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0118-2026 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.
