Centurion Medical recalls CVC Bundle Multimed 3L, 20CM ECVC6060 due to potential fluid droplets separating after disconnection. Affected units sold from 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 CVC Bundle Multimed 3L, 20CM ECVC6060 models because fluid droplets may separate from the connector after disconnection. This could lead to contamination risks during medical procedures.
The BD MaxZeroNeedleless Connector can release fluid droplets when disconnected from the CVC bundle. This separation could potentially contaminate medical equipment or patient sites during procedures.
Healthcare professionals using the CVC bundle for medical procedures are most at risk. Patients receiving care with these devices may also be affected.
Check for the model ECVC6060 on the CVC bundle packaging. These units were sold between 2018 and 2019 with serial numbers starting with 2018032350 through 2019013050.
Look for the model ECVC6060 on the CVC bundle packaging or check the serial numbers listed in the recall notice.
This recall applies to medical devices used in healthcare settings, not home use.
Check the model number ECVC6060 and serial numbers starting with 2018032350 through 2019013050 as listed in the recall notice.
The recall notice does not specify a remedy, so contact Centurion Medical directly for guidance.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0093-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0093-2020 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.
