Centurion Medical recalls CVC bundles with ECVC5120A model due to potential fluid droplets separating after disconnection. Affected units sold in 2018-2019. No remedy specified in recall 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 bundles with model ECVC5120A because fluid droplets might separate from the connector after it's disconnected. This could lead to contamination or infection risks during medical procedures.
The BD MaxZeroNeedleless Connector in the bundle may release fluid droplets when disconnected. This could contaminate the patient or medical equipment if droplets enter the bloodstream during procedures.
Healthcare professionals using these CVC bundles for medical procedures are most at risk. Patients receiving care with these bundles could face infection risks if fluid droplets enter the bloodstream.
Check for the model ECVC5120A on the CVC bundle packaging. These bundles were sold between 2018 and 2019 with serial numbers starting with 2018032350.
Look for serial numbers starting with 2018032350 through 2019013050 on the CVC bundle packaging.
The recall notice does not specify any remedy.
Check for the model ECVC5120A and serial numbers starting with 2018032350 through 2019013050.
Fluid droplets could separate after disconnection, potentially leading to contamination or infection risks during medical 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-0092-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0092-2020 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.
