Centurion Medical recalls UVC Tray UVT875 models from 2017-2018 due to potential fluid droplets separating after disconnection, which could cause contamination. Affected users should contact Centurion for details.
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 UVC Tray UVT875 models made between 2017 and 2018 because fluid droplets might separate from the connector after it's disconnected. This could lead to contamination risks if the device is used improperly.
The UVT875 connector may release fluid droplets when disconnected, which could contaminate surfaces or equipment. This risk is specific to the connector design and does not involve immediate hazards like fire or injury.
Users of the UVC Tray UVT875 models from 2017 to 2018 are likely affected. Healthcare workers and lab personnel using the device for medical purposes are at higher risk due to potential contamination.
Check for the model numbers listed in the recall: 2017051690 through 2018101290. These models were sold between 2017 and 2018.
Look for the model numbers listed in the recall: 2017051690 through 2018101290.
The UVT875 connector may release fluid droplets when disconnected, which could lead to contamination risks.
Check for the model numbers listed in the recall: 2017051690 through 2018101290.
The recall does not specify a remedy, so contact Centurion Medical directly for further instructions.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0107-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0107-2020 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.
