B Braun recalls Perifix FX epidural anesthesia trays with potential incorrect catheter connector lid position. Affected units include specific lot numbers and expiration dates. Contact for remedy details.
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun is recalling certain Perifix FX epidural anesthesia trays due to a risk that the catheter connector lid 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 anesthesia to be delivered incorrectly or not at all, potentially affecting patient safety.
Healthcare professionals using the Perifix FX epidural anesthesia tray with specific lot numbers and expiration dates are most at risk. Patients receiving epidural anesthesia through this equipment may also be affected.
Check for the product code CE17TKFCPS on the tray. Look for lot numbers 0062006314, 0062011670, or 0062028428 and expiration date 07/31/2026.
Identify the product code CE17TKFCPS and lot numbers 0062006314, 0062011670, or 0062028428 on the tray.
The recall is for a potential issue with the catheter connector lid position, which could lead to improper use during epidural procedures. However, the hazard is considered low risk as it does not cause immediate injury.
Check for product code CE17TKFCPS, lot numbers 0062006314, 0062011670, or 0062028428, and expiration date 07/31/2026 on the tray.
The recall 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-0115-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0115-2026 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.
