Centurion Medical recalls Central Line Bundle 16cm Multimed ECVC6545A due to potential fluid droplets separating after disconnection. Affected units sold from 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 a specific central line bundle product because it may cause fluid droplets to separate when disconnected. This could lead to contamination risks during medical procedures. The recall affects units sold starting in 2019 with the model ECVC6545A.
The BD MaxZeroNeedleless Connector in the bundle may allow fluid droplets to separate from the sealed surface after disconnection. This could potentially lead to contamination or infection risks during medical procedures.
Healthcare professionals using the Central Line Bundle 16cm Multimed ECVC6545A for medical procedures are most at risk. Patients receiving treatments through this device could be affected if the product is used.
Check for the model ECVC6545A on the product label. The bundle was sold starting in 2019. The product name is Central Line Bundle 16cm Multimed.
Look for the model ECVC6545A on the product label to confirm if it is affected.
The official recall notice does not specify any remedy.
The product was sold starting in 2019.
The model number is ECVC6545A.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0099-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0099-2020 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.