Centurion Medical recalls facial wound closure trays with specific lot numbers due to potential risk of improper IV placement during use. Affected units include SUT8260A models from 2016-2017.
Convenience Kit containing components to assist practitioner with IV placement and securement.
Centurion Medical is recalling facial wound closure trays (model SUT8260A) because they contain components that could lead to improper IV placement. This poses a risk of complications during medical procedures if not used correctly.
The convenience kit includes components designed to assist with IV placement and securement. If these components are not used correctly, there is a risk of improper IV placement, which could lead to complications during medical procedures.
Healthcare professionals using the recalled facial wound closure trays are most at risk. Patients receiving IV treatments with these trays may experience complications if the components are not properly secured.
Check for the model number SUT8260A on the tray. The affected lot numbers are 2016070490, 2016080590, 2016112990, and 2017090690. These trays were sold between 2016 and 2017.
Look for the model number SUT8260A on the facial wound closure tray.
Confirm the lot number matches the affected numbers: 2016070490, 2016080590, 2016112990, or 2017090690.
The recalled model is SUT8260A.
The affected lot numbers are 2016070490, 2016080590, 2016112990, and 2017090690.
The convenience kit contains components that could lead to improper IV placement during medical procedures if not used correctly.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1098-2018 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-1098-2018 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.