PlainRecalls
FDA Devices Moderate Class II Ongoing

Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System, designed for the surgical environment. 11105200

Reported: November 8, 2023 Initiated: September 12, 2023 #Z-0195-2024

Product Description

Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System, designed for the surgical environment. 11105200

Reason for Recall

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

Details

Units Affected
237 units
Distribution
Nationwide
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System, designed for the surgical environment. 11105200. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 237 units.
Why was this product recalled?
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
Which agency issued this recall?
This recall was issued by the FDA Devices on November 8, 2023. Severity: Moderate. Recall number: Z-0195-2024.