Centurion Medical recalls CVC insertion bundles with potential fluid droplets separating after disconnection. Affected models include ECVC6355 series from 2018-2019. No remedy specified in official notice.
Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Centurion Medical is recalling CVC insertion bundles that may cause fluid droplets to separate after disconnection. This could lead to contamination or infection risks during medical procedures. Affected units have specific model numbers and were sold between 2018 and 2019.
The BD MaxZeroNeedleless Connector in the bundle may release fluid droplets when disconnected from medical equipment. This separation could contaminate the patient or medical environment, increasing infection risk during procedures.
Healthcare professionals using the CVC insertion bundles for medical procedures are most at risk. Patients receiving care through these bundles could face infection risks if fluid droplets separate.
Check for model numbers ECVC6355 with serial numbers starting 2018030250 through 2019040150. These bundles were sold between 2018 and 2019.
Look for model numbers ECVC6355 with serial numbers starting 2018030250 through 2019040150.
The official recall notice does not specify any remedy.
Fluid droplets may separate from the sealed surface, potentially increasing infection risk during medical procedures.
This bundle is used for central venous catheter insertion procedures.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0096-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0096-2020 from Centurion Medical. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
