Centurion Medical recalls CVC bundle models CVI4600 due to potential fluid droplets separating after connector disconnection. Affected units sold in 2019; no remedy specified.
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 labeled CVI4600 because fluid droplets might separate from the connector after it's disconnected. This could lead to contamination risks during medical procedures.
The BD MaxZeroNeedleless Connector can release fluid droplets when disconnected from the CVC bundle. This could potentially contaminate the patient or medical equipment during procedures.
Healthcare providers using the CVI4600 CVC bundle for medical procedures are most at risk. Patients receiving care through these bundles may be affected if the connector is disconnected.
Check for CVC bundles labeled CVI4600 with serial numbers starting with 2019022550 or 2019032250. These were sold in 2019.
Look for serial numbers starting with 2019022550 or 2019032250 on the CVC bundle.
The recall indicates a potential for fluid droplets to separate after disconnection, which could lead to contamination risks during medical procedures.
The recall does not specify a remedy, so check the serial number and contact Centurion Medical if you have the affected model.
Look for CVC bundles labeled CVI4600 with serial numbers starting with 2019022550 or 2019032250, which were sold in 2019.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0079-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0079-2020 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.
