Siemens recalls Cios Spin Image-Intensified Fluoroscopic X-Ray Systems with model VA30-10308194 due to risk of electrical shock from unplugged cables. Affected units may have unsafe voltage at X10 connector.
The unplugging of the main cable on the monitor trolley from the X10 connector can cause an unsafe electrical voltage (up to 67,6 V DC) at the X10 connector. This can result in an electrical shock if the user or other persons touch the contact pins of the X10 connector.
Siemens is recalling specific Cios Spin X-Ray systems because unplugging the main cable from the X10 connector can cause dangerous electrical voltage. This poses a shock risk if someone touches the connector pins. The recall affects units with model number VA30-10308194 and listed serial numbers.
The main cable unplugging from the X10 connector creates unsafe electrical voltage (up to 67.6 V DC) at the connector. If a person touches the contact pins, they could receive an electrical shock.
Medical professionals using the Cios Spin X-Ray system are most at risk. Patients and others near the equipment could also be affected if they touch the connector.
Check for model number VA30-10308194 on the system. Serial numbers listed include 50135, 50131, 50171, 50129, and others. These units were sold with specific serial numbers.
Ensure the main cable is securely connected to the X10 connector to prevent unsafe voltage.
Model number VA30-10308194.
Electrical shock could occur due to unsafe voltage up to 67.6 V DC.
Check for model number VA30-10308194 and serial numbers listed in the recall notice.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2128-2020 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2128-2020 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.
