Centurion Medical recalls pediatric PICC insertion trays CVI4450A due to potential fluid droplets separating after disconnection. Affected units sold in 2018 with specific serial numbers.
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 pediatric PICC insertion trays with model CVI4450A because fluid droplets may separate from the connector after disconnection. This could lead to contamination or infection risks during medical procedures.
The BD MaxZeroNeedleless Connector in the tray can release fluid droplets when disconnected. This separation might cause contamination during medical procedures, potentially increasing infection risks.
Healthcare providers using pediatric PICC insertion trays with model CVI4450A are most at risk. Patients receiving these procedures may also be affected if the trays are used improperly.
Check for the model CVI4450A on the tray. Affected units were sold with serial numbers starting with 2018101250, 2018101850, 2018110950, or 2018121150.
Identify the model number on the tray to confirm if it is CVI4450A.
The BD MaxZeroNeedleless Connector in the tray may release fluid droplets when disconnected, potentially causing contamination during medical procedures.
The recall record does not specify a remedy, so check the model and serial numbers to determine if it is affected.
Yes, affected units have serial numbers starting with 2018101250, 2018101850, 2018110950, or 2018121150.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0077-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0077-2020 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.
