Centurion Medical recalls central venous access device bundle ECVC2840 due to potential fluid droplets separating after disconnection. Affected units sold from 2018-2019. Consumers should contact for remedy.
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 venous access device bundles labeled ECVC2840 because they might release fluid droplets when disconnected. This could lead to contamination or infection risks during medical procedures.
The BD MaxZeroNeedleless Connector in the bundle can separate fluid droplets from its sealed surface when disconnected. This could cause contamination or infection if the droplets come into contact with the patient or environment.
Healthcare professionals using these bundles for medical procedures are most at risk. Patients receiving treatments with these devices may also be affected.
Check for the ECVC2840 label on the central venous access device bundle. These units were sold between 2018 and 2019.
Reach out to Centurion Medical for instructions on how to return or replace the recalled bundle.
The recall states the hazard occurs after disconnection, so it should be safe during normal use if handled properly.
Look for the ECVC2840 label on the central venous access device bundle, which was sold between 2018 and 2019.
Contact Centurion Medical for instructions on returning or replacing the bundle.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0089-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0089-2020 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.
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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.
