Centurion Medical recalls CAP CHANGE KIT DYNDC1496B due to potential fluid droplets separating after disconnection. Affected units sold from 2018-2019. No remedy specified in official 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 their CAP CHANGE KIT DYNDC1496B because fluid droplets might separate from the connector after it's disconnected. This could pose a risk of exposure to bodily fluids during medical procedures.
The BD MaxZeroNeedleless Connector in the kit can release fluid droplets when disconnected. This could lead to exposure to bodily fluids if proper precautions aren't taken during medical procedures.
Healthcare professionals using the CAP CHANGE KIT DYNDC1496B for medical procedures are most at risk. Patients receiving care with this kit may also be exposed.
Check for the model number DYNDC1496B on the kit. The product was sold between 2018 and 2019.
Look for the model number DYNDC1496B on the kit packaging or label.
The recall states there is a potential for fluid droplets to separate after disconnection, which could pose a risk during medical procedures. However, no specific remedy is provided in the official notice.
The official recall notice does not specify any action steps. You should check the model number and contact Centurion Medical for further guidance.
The product was sold between 2018 and 2019 based on the serial numbers 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-0083-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0083-2020 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.
