Centurion Medical recalls Central Line Bundle 16cm Multimed ECVC6545 due to potential fluid droplets separating after disconnection. Affected units sold in 2018 with specific serial numbers.
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 Line Bundle 16cm Multimed ECVC6545 kits because fluid droplets may separate from the connector after disconnection. This could lead to contamination risks during medical procedures.
The BD MaxZeroNeedleless Connector in the kit can release fluid droplets when disconnected. This separation could cause contamination during medical procedures if not properly managed.
Healthcare professionals using the Central Line Bundle 16cm Multimed ECVC6545 kits for medical procedures are most at risk. Patients receiving care through these kits may also be affected.
Check for the model ECVC6545 on the kit. Units sold with serial numbers 2018102950 or 2018110250 from 2018 are affected.
Look for serial numbers 2018102950 or 2018110250 on the Central Line Bundle 16cm Multimed ECVC6545 kit.
The recall is for potential fluid droplet separation after disconnection, which could lead to contamination risks during medical procedures. It is not described as causing serious injury.
Check the serial numbers on the kit. If it matches 2018102950 or 2018110250, contact Centurion Medical for instructions.
Affected kits have the model ECVC6545 and serial numbers 2018102950 or 2018110250, sold in 2018.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0098-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0098-2020 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.
