Centurion Medical recalls Central Line Bundle ECVC6375 due to potential droplets separating from the connector after disconnection. Affected units sold in 2018-2019; stop using immediately.
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 Central Line Bundle ECVC6375 kits because fluid droplets may separate from the connector after disconnection. This could lead to contamination or infection risks during medical procedures. Affected units were sold between September 2018 and January 2019.
The BD MaxZeroNeedleless Connector may release fluid droplets when disconnected from the central line bundle. This separation could introduce contaminants into the bloodstream or cause infections during medical procedures.
Healthcare professionals using the Central Line Bundle ECVC6375 for medical procedures are most at risk. Patients receiving treatments through these bundles could be exposed to potential contamination.
Check for the model ECVC6375 on the bundle packaging. Units were sold between September 2018 and January 2019 with serial numbers starting with 2018091150, 2018101050, 2018121950, or 2019010950.
Discontinue use of the Central Line Bundle ECVC6375 as it poses a contamination risk.
The recalled model is ECVC6375.
Units were sold between September 2018 and January 2019.
Check the model number on the packaging; affected units have the ECVC6375 model and serial numbers starting with 2018091150, 2018101050, 2018121950, or 2019010950.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0097-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0097-2020 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.
