B Braun recalls Perifix FX epidural anesthesia trays with potential incorrect catheter connector lid position. Affected units sold through medical suppliers until July 2026.
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 risk is specific to medical settings where precise equipment handling is critical.
Healthcare professionals using the recalled Perifix FX epidural trays for anesthesia procedures are most at risk. Patients receiving these procedures may be affected if the equipment is used incorrectly.
Check for the product code CE17TKFCS on the tray. The lot numbers listed (0062013051 through 0062013053) and expiration date of July 31, 2026 indicate the affected units.
Verify the product code CE17TKFCS and lot numbers on the tray to confirm if it's affected.
The recall indicates a potential risk with the lid position, but the product is generally safe if used correctly. Affected units should be checked for the specific lot numbers listed.
Check for the product code CE17TKFCS and lot numbers 0062013051 through 0062013053. The expiration date is July 31, 2026.
The recall does not specify a remedy, so contact B Braun directly for guidance on handling the affected units.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0119-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0119-2026 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.
