B. Braun recalls specific catheter connectors that may leak or disconnect during use, posing a risk of infection or improper fluid delivery. Affected units include certain batch numbers sold for medical use.
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 specific catheter connectors that may leak or disconnect during medical procedures. This could lead to improper fluid delivery or infection risks for patients receiving anesthesia.
The catheter connectors may not stay securely closed, leading to potential leakage or disconnection of catheters. This can cause improper fluid delivery or infection risks during medical procedures.
Physicians using the recalled catheter connectors for anesthesia and fluid administration are most at risk. Patients receiving procedures with these connectors may also face complications.
Check for the model NES1727KFX W /17GA TUOHY 19GA SPRW OT with Material Number 333197. Affected units were sold in batches: 61587099, 61591814, 61603113, 61606091, 61615215, 61618399.
Identify the model NES1727KFX W /17GA TUOHY 19GA SPRW OT with Material Number 333197 to confirm if your connector is affected.
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of catheters.
Batches 61587099, 61591814, 61603113, 61606091, 61615215, and 61618399 are affected.
The recall does not specify a stop-use instruction; however, you should check if your connector is affected before use.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3395-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3395-2018 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.
