Siemens recalls certain SOMATOM go.Top CT scanners with specific software versions due to potential workflow interruptions and delays in patient scans. Affected units may require attention to avoid diagnostic delays.
The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. This may cause a delay in diagnosis or patient scans.
Siemens is recalling specific models of SOMATOM go.Top CT scanners that have software versions VA20A, VA20A_SP0, or VA20_SP1. These scanners could cause delays in patient scans and diagnosis if the software has sporadic performance issues.
The software versions in question may cause intermittent workflow interruptions and unexpected notifications during scans. This could lead to delays in diagnosis or patient scans, but does not pose a direct safety risk to users.
Healthcare facilities using the recalled CT scanners are most at risk, particularly those providing diagnostic imaging services. Patients undergoing scans on these units may experience delays in their care.
Check for the model number 1161640 on the scanner and software versions VA20A, VA20A_SP0, or VA20_SP1. Serial numbers listed include 119103, 119090, 119098, and others as detailed in the recall notice.
Verify the software version on your SOMATOM go.Top scanner to see if it is VA20A, VA20A_SP0, or VA20_SP1.
The model number is 1161640.
Software versions VA20A, VA20A_SP0, and VA20_SP1 are affected.
No, the recall does not require immediate discontinuation. Users can continue using the scanner but should check for software updates.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1918-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1918-2019 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.
