Angiodynamics recalls specific Solero MTA Generator models with serial numbers QBY0002623 to QBY0002745 due to potential Error 0001 during system start-up. Affected units require software upgrade to reduce this issue.
Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up.
Angiodynamics is recalling specific Solero MTA Generator models with certain serial numbers because they may experience Error 0001 during system start-up. This issue requires a software upgrade to prevent the error from occurring.
The generator may display Error 0001 during system start-up if the software is not updated. This error could occur in normal use without causing harm, but it indicates a potential need for software correction.
Owners of the Solero MTA Generator with specific serial numbers listed in the recall notice are affected. Users who have these units are most at risk of encountering Error 0001 during start-up.
Check the serial number on your Solero MTA Generator. Affected units have serial numbers starting with QBY0002 and ending with numbers from 0002363 to 0002745 as listed in the recall notice.
Identify your Solero MTA Generator's serial number to see if it is listed in the recall notice.
Reach out to Angiodynamics for software upgrade instructions if your unit is affected.
Error 0001 is a potential issue that can occur during system start-up of the Solero MTA Generator if the software is not updated.
No, the recall does not require stopping use; affected units need a software upgrade to reduce the error.
Check the serial number against the list of affected numbers provided in the recall notice.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2439-2021 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2439-2021 from Angiodynamics. 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.
