B. Braun recalls CNB400TU3KUE 18GX4 Ultra 360 catheter connectors due to potential leakage or disconnection during use. Affected units have batch number 61602050. Contact for replacement.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
B. Braun is recalling a specific catheter connector model because it can leak or disconnect during medical procedures. This could lead to improper anesthetic delivery or infection risks for patients.
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of the catheter from the connector. This could cause improper anesthetic delivery or infection risks during medical procedures.
Physicians using the CNB400TU3KUE 18GX4 Ultra 360 catheter connector with batch number 61602050 are affected. Medical facilities using this connector for anesthetic delivery are most at risk.
Check for the model number CNB400TU3KUE 18GX4 Ultra 360 with batch number 61602050. This connector is used by physicians for anesthetic and fluid administration.
Look for the batch number 61602050 on the connector.
Reach out to B. Braun Medical for replacement or guidance on next steps.
The recall indicates potential leakage or disconnection during use, which could lead to improper anesthetic delivery or infection risks. However, the remedy does not specify immediate stop-use.
Check for the model number CNB400TU3KUE 18GX4 Ultra 360 with batch number 61602050. This connector is used by physicians for anesthetic and fluid administration.
Contact B. Braun Medical for replacement or guidance. The recall does not specify a deadline for action.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3349-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3349-2018 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.
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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.
