Centurion Medical recalls INFUSA Port Kit DYNDC1840F due to potential fluid droplets separating after disconnection. Affected units sold from 2018-2019. Stop using immediately to prevent injury.
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 INFUSA Port Kit DYNDC1840F because fluid droplets may separate from the connector after disconnection. This could lead to contamination or injury if not handled properly. Affected units have serial numbers starting with 2018092090 through 2019032790.
The BD MaxZeroNeedleless Connector in the kit may release fluid droplets when disconnected. This could cause contamination or injury if the droplets come into contact with the user or environment.
Patients using the INFUSA Port Kit DYNDC1840F for medical treatments are most at risk. The recall affects individuals with the specific serial numbers listed in the product description.
Check for serial numbers starting with 2018092090, 2018100890, 2018122890, or 2019032790 on the INFUSA Port Kit DYNDC1840F. These units were sold between 2018 and 2019.
Discontinue use of the INFUSA Port Kit DYNDC1840F with the affected serial numbers to prevent potential fluid droplet exposure.
Fluid droplets may separate from the connector after disconnection, potentially causing contamination or injury.
Serial numbers starting with 2018092090, 2018100890, 2018122890, or 2019032790.
Look for the serial numbers listed in the product description: 2018092090, 2018100890, 2018122890, or 2019032790.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0085-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0085-2020 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.
