Angiodynamics recalls specific Solero MTA Generator refurbished units with serial numbers QBY0002816-QBY0002858 due to potential Error 0001 during startup. No immediate action required as software update resolves the 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 refurbished Solero MTA Generators with certain serial numbers because they need a software update to prevent Error 0001 during startup. This recall does not pose an immediate safety risk to users.
The generator may display Error 0001 during startup if the software is not updated. This error occurs due to outdated software in the specific refurbished units that require a software upgrade to prevent it.
Users of the Solero MTA Generator refurbished units with serial numbers QBY0002816 through QBY0002858 are affected. These units were sold as refurbished products with specific software versions.
Check your Solero MTA Generator's serial number against the list: QBY0002816, QBY0002817, QBY0002348, QBY0002308, QBY0002311, QBY0002711, QBY0002741, QBY0002858.
Verify your generator's software version to confirm if it needs an update to prevent Error 0001.
No, the recall does not require stopping use. The generator can be used after updating the software.
Error 0001 is a startup issue that occurs in specific refurbished units with outdated software.
The official recall does not specify how to obtain the software update; contact Angiodynamics for instructions.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2438-2021 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2438-2021 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.
