Centurion Medical recalls its TRIDM250 Outpatient Driveline Mgmt System due to incomplete sterile packaging that could compromise sterility. Affected units sold from 2019. No remedy specified in official notice.
Incomplete seals on the sterile package may compromise the sterility
Centurion is recalling its TRIDM250 Outpatient Driveline Management System because the sterile packaging might not seal properly, risking contamination. This could lead to infections if the device is used without proper sterility.
The sterile packaging may not seal completely, allowing contaminants to enter the system. This could lead to infections if the device is used without proper sterility during medical procedures.
Healthcare providers using the Centurion TRIDM250 Outpatient Driveline Management System for patient care are likely affected. Patients receiving treatment with this system are at risk if sterility is compromised.
Check for the product name 'TRIDM250 Outpatient Driveline Mgmt System' from Centurion Medical. Units were sold starting from 2019.
Identify the product name and model number to confirm if it matches the recalled item.
The official recall notice does not specify any remedy.
Check for the product name 'TRIDM250 Outpatient Driveline Mgmt System' from Centurion Medical. Units were sold starting from 2019.
The official recall notice does not specify any remedy.
We’ve drafted a message you can send Centurion to request your refund or repair — edit it as you like.
Subject: Recall Z-1071-2020 — Centurion Centurion Hello, I own a Centurion that is covered by recall Z-1071-2020 from Centurion. 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.
