B Braun Perifix FX Epidural Tray Recall: Incorrect Lid Position Hazard

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Contact the company & request your remedy

Recalling firmB BRAUN MEDICAL INC861 Marcon Blvd · Allentown, PA 18109-9577

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

B Braun is recalling Perifix FX continuous epidural anesthesia trays that may have the catheter connector lid in the wrong position. This could lead to improper use during medical procedures if not corrected.

Why it’s dangerous

The catheter connector lid might be in the wrong position, which could cause improper use during epidural anesthesia procedures. This might lead to incorrect medication delivery or other complications if not fixed.

Who’s affected

Healthcare professionals using the Perifix FX epidural anesthesia tray for procedures are most at risk. Patients receiving epidural anesthesia through this device may be affected.

How to tell if you have this one

Check for the product code CE17TKF on the tray. The affected units were sold with expiration date 07/31/2026.

Brand
B Braun
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Lid Position
Inspect the catheter connector lid to ensure it is correctly positioned before use.

✎ GovInfoNow

Questions people ask

Is this recall for patients or healthcare providers?

This recall is for healthcare providers using the Perifix FX epidural anesthesia tray during procedures.

What is the product code for the recalled items?

The product code is CE17TKF.

How can I tell if I have the recalled item?

Check for product code CE17TKF with expiration date 07/31/2026.

Take action

Contact B Braun

We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0117-2026 — B Braun B Braun

Hello,

I own a B Braun that is covered by recall Z-0117-2026 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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Where this comes from

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.

Official source: FDA Recall #Z-0117-2026 (September 18, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0117-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged

Use caution until it’s fixed