Siemens recalls Cios Alpha (VA30) mobile X-ray systems due to software issues that could lead to patient misdiagnosis or repeat imaging. Affected units have specific serial numbers.
Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems, fulfillment of new requirements from DIN and IEC standards for Cios VA30 systems required may result in patient misdiagnosis/repeat exposure
Siemens is recalling its Cios Alpha (VA30) mobile X-ray systems because a software issue might cause patient misdiagnosis or repeat imaging. This affects medical facilities using the equipment for surgeries.
The software issue in the Cios Alpha, Cios Flow, and Cios Spin VA30 systems may not fulfill new standards from DIN and IEC, leading to incorrect imaging results. This could cause patients to be misdiagnosed or require repeat imaging.
Medical facilities that use the Siemens Cios Alpha (VA30) mobile X-ray systems for surgical procedures are affected. Patients undergoing imaging with these systems could face misdiagnosis or repeated scans.
Check for the serial numbers listed in the recall notice: 40013 to 40276 and 43000 to 43339. The equipment is designed for surgical environments and is used in hospitals.
Verify if your Siemens Cios Alpha (VA30) mobile X-ray system has a serial number from the list provided in the recall notice.
The software issue may not meet new DIN and IEC standards for Cios VA30 systems, which could lead to patient misdiagnosis or repeat imaging.
Check if your unit has a serial number from the list provided in the recall notice. If it does, contact Siemens for further instructions.
Yes, patients could be misdiagnosed or require repeat imaging due to the software issue, but the recall does not require immediate discontinuation of use.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0195-2024 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0195-2024 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.
