Centurion Medical recalls OR VANTEX 7FR 3L 16CM CVC ECVC6665 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 OR VANTEX 7FR 3L 16CM CVC ECVC6665 catheters because fluid droplets may separate from the connector after disconnection. This could lead to contamination or infection risks during medical procedures.
The connector can release fluid droplets when disconnected, potentially causing contamination. This poses a risk of infection or cross-contamination during medical procedures if not handled properly.
Healthcare professionals using the OR VANTEX catheters are most at risk. Patients receiving these catheters may also be affected if the device is used improperly.
Check for the model number ECVC6665 on the OR VANTEX 7FR 3L 16CM CVC catheter. Units were sold between 2018 and 2019 with serial numbers starting with 2018111950, 2019031350, or 2019040550.
Look for serial numbers starting with 2018111950, 2019031350, or 2019040550 on the catheter.
The product is not safe for use as it may release fluid droplets after disconnection, posing infection risks. Affected units should be recalled.
Check for the model number ECVC6665 and serial numbers starting with 2018111950, 2019031350, or 2019040550.
The recall does not specify a remedy, so contact Centurion Medical for guidance on safe disposal or replacement.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0100-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0100-2020 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.
