Angiodynamics recalls refurbished Solero MTA Generators with specific serial numbers due to potential Error 0001 during startup. Affected units require software upgrade to prevent issues.
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 refurbished Solero MTA Generators with certain serial numbers because they need a software update to reduce the chance of Error 0001 occurring during startup. This recall is important because the error could cause system issues if not fixed.
The generators require a software update to prevent Error 0001 from happening during startup. This error could cause system issues if the software is not upgraded.
Owners of the recalled Solero MTA Generators with specific serial numbers listed in the recall notice. Users who operate these generators for medical purposes may be most at risk.
Check the serial number on your Solero MTA Generator. The affected units have specific serial numbers listed in the recall notice: QBY0002546, QBY0002517, QBY0002525, QBY0002562, QBY0002669, QBY0002569, QBY0002382, QBY0002682, QBY0002561, QBY0002567, QBY0002580, QBY0002398, QBY0002379, QBY0002612, QBY0002708, QBY0002527, QBY0002758, QBY0002552.
Identify your Solero MTA Generator's serial number to see if it is listed in the recall notice.
Reach out to Angiodynamics for software update instructions if your unit is affected.
The recall is for specific serial numbers of the Solero MTA Generator that require a software update to reduce the chance of Error 0001 occurring during startup.
Check the serial number against the list provided in the recall notice: QBY0002546, QBY0002517, QBY0002525, QBY0002562, QBY0002669, QBY0002569, QBY0002382, QBY0002682, QBY0002561, QBY0002567, QBY0002580, QBY0002398, QBY0002379, QBY0002612, QBY0002708, QBY0002527, QBY0002758, QBY0002552.
No, the recall does not require stopping use. Affected units need a software update to prevent Error 0001 during startup.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2436-2021 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2436-2021 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.
