Siemens recalls ARTISTE MV System Model #8139789 with specific software versions due to potential radiation overdose risk in radiation therapy. Affected units may require correction to prevent 10-20% overdose.
Potential safety issue with the dose monitoring system safety interlocks which could result in a 10-20% overdose of radiation therapy.
Siemens is recalling ARTISTE MV System Model #8139789 with certain software versions because a dose monitoring issue could cause radiation therapy overdoses. This affects medical equipment used in cancer treatment facilities.
The dose monitoring system safety interlocks in the ARTISTE MV System software versions 6, 7, 9, and 13 may not function correctly, leading to radiation therapy overdoses. This could result in a 10-20% higher radiation dose than intended for patients.
Healthcare facilities using the ARTISTE MV System with the specified software versions are most at risk. Patients receiving radiation therapy through this equipment could potentially receive a 10-20% overdose.
Check if your ARTISTE MV System has model number 8139789 and software versions 6, 7, 9, or 13. Serial numbers listed in the recall include 5350, 5410, 5419, and others.
Verify your ARTISTE MV System software version by checking the console display or documentation.
Reach out to Siemens Medical Solutions for guidance on next steps and potential software updates.
The recall addresses a potential safety issue that could result in a 10-20% radiation overdose, but the risk is not immediate for all users.
Check if your ARTISTE MV System has model number 8139789 and software versions 6, 7, 9, or 13. Serial numbers listed in the recall include 5350, 5410, 5419, and others.
The recall does not require immediate discontinuation; affected facilities should contact Siemens for guidance on corrective actions.
We’ve drafted a message you can send Siemens Medical Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-1677-2020 — Siemens Medical Solutions Siemens Medical Solutions Hello, I own a Siemens Medical Solutions that is covered by recall Z-1677-2020 from Siemens Medical Solutions. 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.
