Centurion Medical recalls IV kit IVS3405 due to potential fluid droplets separating after disconnection. Affected units sold from 2017-2019; check serial numbers listed.
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 IV kits with model IVS3405 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 kit may release fluid droplets when disconnected. This could cause contamination if the droplets come into contact with the patient or the medical environment.
Healthcare professionals using the IV kit for medical procedures are most at risk. Patients receiving IV treatments with this kit could face infection risks if droplets enter the bloodstream.
Check for the model number IVS3405 on the kit. Serial numbers listed in the recall include 2019031490 through 2019020690, sold between 2017 and 2019.
Look for the model number IVS3405 on the IV kit packaging or label.
Reach out to Centurion Medical for assistance with the recall process.
The recall states the kit may release fluid droplets after disconnection, so it is not recommended for use until the recall is addressed.
Check the model number and serial numbers listed in the recall to confirm if your kit is affected. Contact Centurion Medical for further instructions.
The affected kits have model number IVS3405 and serial numbers from 2017100690 through 2019020690, sold between 2017 and 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-0103-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0103-2020 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.
