Cios Alpha (2019-03-18)

Starting date:

March 18, 2019

Posting date:

April 29, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-69772

Last updated: 2019-04-30

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  Reason
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  Affected products

Affected Products

Cios Alpha

Reason

The organ programs pre-installed ex works enable safe operation within the specified performance limits. However, it is possible to overwrite the organ programs with higher performance parameters.

Affected products