B. Braun Medical CNB200TKU Catheter Kit Recall: Risk of Catheter Leakage

Take action

Contact the company & request your remedy

Recalling firmB. Braun Medical, Inc.901 Marcon Blvd · Allentown, PA 18109-9512

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

B. Braun is recalling certain non-stim catheter kits that may leak or disconnect during use. This could lead to fluid leaks or improper administration of anesthetic. Affected kits should be checked for the specific batch numbers listed.

Why it’s dangerous

The catheter connectors may not stay closed properly, leading to leakage or disconnection of the catheter from the connector. This can cause fluid leaks or improper administration of anesthetic during medical procedures.

Who’s affected

Physicians using the CNB200TKU non-stim catheter kits with batch numbers 61596337, 61604:11, or 61610323 are most at risk. These kits are used for administering anesthetics and fluids during medical procedures.

How to tell if you have this one

Check the product label for the batch numbers: 61596337, 61604211, or 61610323. The product is a non-stim catheter kit used by physicians for anesthetic and fluid administration.

Brand
B. Braun
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for batch numbers 61596337, 61604211, or 61610323 on the catheter kit.

✎ GovInfoNow

Questions people ask

What is the hazard with this catheter kit?

The catheter connectors may not stay closed, leading to leakage or disconnection of the catheter during use.

Which batch numbers are affected?

Batch numbers 61596337, 61604211, and 61610323.

What should I do if I have this kit?

Check the product label for the batch numbers. If affected, contact B. Braun Medical for return instructions.

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-3345-2018 — B. Braun B. Braun

Hello,

I own a B. Braun that is covered by recall Z-3345-2018 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-3345-2018 (July 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3345-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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 CNB200TKU NON-STIM CATH FULL KIT, Material Number 332127 Connection device used by physicians to provide various

Use caution until it’s fixed