Cios Spin, Cios Flow, and Cios Alpha
Brand(s)
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
Get notified
Receive notifications for new and updated recalls and alerts by category.