Siemens recalls specific Artis Q angiography system models (10848280-10848355) due to potential thermal effects that could damage system parts. Affected units include detailed serial numbers for each model.
Potential hardware issue which may cause thermal effects and possible damage to system parts.
Siemens is recalling specific models of Artis Q angiography systems that may experience thermal issues causing damage to internal components. This recall affects medical imaging equipment used in hospitals and clinics for procedures like cardiac and neuro angiography.
The recall states there is a potential hardware issue that may cause thermal effects, which could lead to damage of system parts. This is a thermal issue that might affect the internal components of the angiography system during operation.
Healthcare facilities using the recalled Artis Q angiography systems (models 10848280-10848355) are most at risk. These systems are used for diagnostic imaging and interventional procedures in hospitals and clinics.
Check if your Artis Q angiography system has one of the model numbers listed (10848280, 10848281, 10848282, 10848283, 10848353, 10848354, or 10848355). Each model has specific serial numbers provided in the recall notice.
Verify your Artis Q angiography system model number against the list of affected models (10848280-10848355) provided in the recall notice.
The recall states there is a potential hardware issue that may cause thermal effects, which could damage system parts.
Check if your Artis Q angiography system has one of the model numbers listed (10848280-10848355) and compare the serial numbers to the detailed lists provided in the recall notice.
If your system model is not listed, it is not affected by this recall and no action is required.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2747-2018 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2747-2018 from Siemens. 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.
