B Braun recalls Perifix FX epidural anesthesia sets due to potential incorrect catheter connector lid position. Affected units include specific model 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 Perifix FX continuous epidural anesthesia sets because the catheter connector lid might be in the wrong position. This could lead to improper use during medical procedures. Affected products have specific model numbers and lot dates.
The catheter connector lid may not be properly aligned, which could cause improper fluid flow during epidural anesthesia administration. This might lead to incorrect dosing or complications if the lid is not correctly positioned.
Medical professionals using the Perifix FX epidural sets for anesthesia procedures. Patients receiving epidural anesthesia from these sets are at risk if the connector lid is mispositioned.
Check for the product code CE17TFC on the packaging. The affected units have lot number 0062014626 and expire May 31, 2028. The product includes a specific epidural needle and catheter combination.
Look for product code CE17TFC and lot number 0062014626 on the packaging.
The catheter connector lid may be in the incorrect position, which could lead to improper fluid flow during epidural anesthesia administration.
Check for product code CE17TFC and lot number 0062014626 on the packaging. The product expires May 31, 2028.
The recall record does not specify a remedy, so contact B Braun directly 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-0121-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0121-2026 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.
