S-Series Equipment Management Syetem (2021-02-02)

Starting date:

February 2, 2021

Posting date:

February 19, 2021

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

Healthcare Professionals, General Public, Hospitals

Identification number:

RA-75011

Last updated: 2021-02-19

• Reason
• Affected products

Affected Products 

S-Series Equipment Management Syetem

Reason

Stryker has become aware that there is a likelihood that the S-Series Equipment Management System Capacitive Touch Controls on the MFRs rotational electrical magnetic brakes may disengage with the use of an electrocautery device. The potential hazard associated is the boom may experience unintentional horizontal drifting with the use of an electrocautery device that could lead to patient injury needing medical/surgical intervention.

Affected products