Health product recall

Cios Spin, Cios Flow, and Cios Alpha

Last updated

Summary

Product
Cios Spin, Cios Flow, and Cios Alpha
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Cios Spin

53044
53149
50175
50423
52083
53036
52096

10308194

Cios Flow

82225
83262
83415
83167

11108110

Cios Alpha

40211
40269
43203
42047
43066

11105200

Issue

Siemens has become aware of a potential software issue for users of Cios Alpha, Cios Flow, and Cios Spin VA30 systems. Due to a software issue, fulfillment of new requirements from DIN and IEC standards for Cios VA30 systems is necessary. With software version VA30K, the user interface of Cios VA30 systems will be changed to consider the current standards DIN 6862-3 and IEC 60601-2-54.

Recall Start Date: October 11, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies

Siemens Healthcare Gmbh

Henkestr. 127, Erlangen, Germany, 91052

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74441

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