Siemens Medical recalls specific MEVATRON radiation therapy models due to potential 10-20% overdose risk from dose monitoring system failures.
Potential safety issue with the dose monitoring system safety interlocks which could result in a 10-20% overdose of radiation therapy.
Siemens Medical is recalling several MEVATRON radiation therapy models because their dose monitoring system might cause a 10-20% overdose of radiation during treatment. This could lead to serious health effects if the system fails during use.
The dose monitoring system safety interlocks in these devices could malfunction, leading to a 10-20% overdose of radiation therapy. This risk occurs during treatment when the system fails to properly monitor radiation delivery.
Patients receiving radiation therapy using the recalled MEVATRON models are most at risk. Healthcare facilities that use these devices for treatment may also be affected.
Check for the model numbers listed in the recall: MEVATRON M2/Primus Mid-Energy #01940035, MEVATRON PRIMART #05500371, MEVATRON KD-2 #08515520, and MEVATRON KD2 #01940753. Also look for specific software versions 6, 7, 9, 13 and the listed serial numbers.
Identify your MEVATRON model number and software version to see if it matches the recalled items.
Reach out to Siemens Medical Solutions USA, Inc. for guidance on next steps if your device is affected.
The dose monitoring system safety interlocks in these devices could malfunction, potentially causing a 10-20% overdose of radiation therapy during treatment.
MEVATRON M2/Primus Mid-Energy #01940035, MEVATRON PRIMART #05500371, MEVATRON KD-2 #08515520, MEVATRON KD2 #01940753, and other specific models with listed software versions and serial numbers.
No, but you should check if your device is affected and contact Siemens Medical Solutions USA, Inc. for further instructions.
We’ve drafted a message you can send Siemens Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1678-2020 — Siemens Medical Siemens Medical Hello, I own a Siemens Medical that is covered by recall Z-1678-2020 from Siemens Medical. 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.
