Centurion Medical recalls SORBAVIEW IVS3475 IV kits after potential fluid droplets separate from connectors during disconnection. Affected units sold in 2018-2019. No remedy specified in recall notice.
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 SORBAVIEW IVS3475 IV kits because fluid droplets may separate from the connector after disconnection. This could lead to contamination or infection risks during medical procedures. The recall affects kits sold between 2018 and 2019.
The BD MaxZeroNeedleless Connector in the kit may release fluid droplets when disconnected. This could contaminate the IV fluid or the patient's bloodstream, increasing infection risk during medical procedures.
Healthcare professionals using IV kits for medical procedures are most at risk. Patients receiving IV treatments with these kits could face infection risks if droplets contaminate the fluid.
Check for the SORBAVIEW IVS3475 model number on the kit packaging. Affected kits were sold between 2018 and 2019 with specific serial numbers listed in the recall notice.
Review the serial numbers on the kit packaging to confirm if it matches the affected models listed in the recall notice.
The recall notice does not specify a remedy or fix for this issue.
The affected kits are SORBAVIEW IVS3475 models with serial numbers starting with 2018 or 2019 as listed in the recall notice.
Check the serial numbers on the kit packaging against the list of affected models provided in the recall notice.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0104-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0104-2020 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.
