Centurion Medical recalls invasive procedure tray MNS9510 due to potential fluid droplets separating after disconnection. Affected units sold in 2017; 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 their invasive procedure tray model MNS9510 because it may cause fluid droplets to separate after being disconnected. This could lead to contamination risks during medical procedures.
The BD MaxZeroNeedleless Connector in the tray may release fluid droplets when disconnected. This could potentially contaminate the procedure area or equipment, increasing infection risk during medical treatments.
Healthcare professionals using the tray during medical procedures are most at risk. Patients receiving care with this tray could also be affected.
Check for the model number MNS9510 on the tray. Units were sold starting in 2017 with serial numbers 2017100990 and 2017120490.
Identify the model number on the tray to confirm if it matches MNS9510.
The recall record does not specify a remedy.
The recall record does not specify a remedy.
Units were sold starting in 2017 with serial numbers 2017100990 and 2017120490.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0105-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0105-2020 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.
