Centurion Medical recalls TRIPLE LUMEN BUNDLE KIT ECVC1540 due to potential fluid droplets separating after disconnection. Affected units sold from 2017-2019.
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 its TRIPLE LUMEN BUNDLE KIT ECVC1540 because fluid droplets may separate from the connector after disconnection. This could lead to contamination risks during medical procedures.
The BD MaxZeroNeedleless Connector may release fluid droplets when disconnected from the kit. This could cause contamination during medical procedures if the droplets come into contact with sterile surfaces or patients.
Healthcare professionals using the kit for medical procedures are most at risk. Patients receiving care with this kit could be exposed to potential contamination.
Check for the model ECVC1540 on the kit packaging. Units were sold between 2017 and 2019 with serial numbers listed in the recall notice.
Look for serial numbers 2017102650 through 2019032250 on the kit packaging.
The recall states the connector may release fluid droplets after disconnection, but no specific remedy is provided. Users should check if their kit has the listed serial numbers.
The recall does not specify a remedy, so users should check if their kit has the listed serial numbers and contact Centurion Medical for further guidance.
The kits were sold between 2017 and 2019, as indicated by the serial numbers 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-0088-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0088-2020 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.
