Centurion Medical recalls neonatal PICC catheters CVI4535 due to potential fluid droplets separating after disconnection. Affected units sold from 2019-02-0190. No remedy specified in recall 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 neonatal PICC catheters model CVI4535 because fluid droplets may separate from the connector after disconnection. This could pose a risk during medical procedures for infants.
The BD MaxZeroNeedleless Connector in the catheter kit can release fluid droplets when disconnected. This separation could potentially contaminate the procedure site during infant medical treatments.
Healthcare providers using neonatal PICC catheters model CVI4535 are most at risk. Infants receiving these catheters during medical procedures may be affected.
Check for the model number CVI4535 on neonatal PICC catheters. Units were distributed starting February 2019 (date code 2019020190).
Look for the model number CVI4535 on the neonatal PICC catheter kit.
The BD MaxZeroNeedleless Connector in the kit may release fluid droplets when disconnected, potentially contaminating the procedure site during infant medical treatments.
The recall notice does not specify a remedy or fix for this issue.
Check for the model number CVI4535 on neonatal PICC catheters. Units were distributed starting February 2019 (date code 2019020190).
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0078-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0078-2020 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.
