Centurion Medical recalls VANTEX 7FR CVC Bundles ECVC6670 due to potential fluid droplets separating after disconnection. Affected units sold in 2018-2019.
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 VANTEX 7FR CVC Bundles with model ECVC6670 because fluid droplets might separate from the connector after it's disconnected. This could lead to contamination or infection during medical procedures.
The BD MaxZeroNeedleless Connector in the bundle may release fluid droplets when disconnected. This could contaminate the patient or equipment, increasing infection risk during medical procedures.
Healthcare professionals using the VANTEX 7FR CVC Bundle ECVC6670 for medical procedures are most at risk. Patients receiving care through this equipment could be affected if the recall is not addressed.
Check for the model ECVC6670 on the VANTEX 7FR CVC Bundle. Units were sold between 2018 and 2019 with serial numbers starting with 2018111950, 2019031350, or 2019040550.
Look for the model ECVC6670 on the VANTEX 7FR CVC Bundle to confirm if it's affected.
Reach out to Centurion Medical for specific guidance on handling the recalled bundle.
The product is not safe for use as it may release fluid droplets after disconnection, increasing infection risk. Contact Centurion Medical for specific instructions.
Check for the model ECVC6670 and contact Centurion Medical for guidance on handling the recalled bundle.
Units were sold between 2018 and 2019 with serial numbers starting with 2018111950, 2019031350, or 2019040550.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0101-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0101-2020 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.
