Centurion Medical recalls CVC bundles with ECVC5095 model due to potential fluid droplets separating after disconnection. Affected units sold in 2018. Contact for return instructions.
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 ECVC5095 because fluid droplets may 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 bloodstream or cause infections during medical procedures if droplets enter the patient's system.
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 ECVC5095 on the CVC bundle packaging. These units were sold starting in 2018 with serial numbers like 2018031450.
Look for the model ECVC5095 on the CVC bundle packaging or label.
Reach out to Centurion Medical for specific return or replacement instructions.
The BD MaxZeroNeedleless Connector in the bundle may release fluid droplets when disconnected, potentially causing contamination or infection risks during medical procedures.
Check for the model ECVC5095 on the CVC bundle packaging. These units were sold starting in 2018 with serial numbers like 2018031450.
Contact Centurion Medical for specific return or replacement instructions.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0090-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0090-2020 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.
