Combi Suite Angio Transfer Board (2018-11-29)

Starting date:

November 29, 2018

Posting date:

January 8, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-68680

• Reason
• Affected products

Affected products

Combi Suite Angio Transfer Board

Reason

The springs, screws and threaded inserts in both handles of the transfer boards are magnetic and can cause signal loss in the region of knee and foot. The artifacts will be clearly recognizable. The impacted handles will be exchanged.

Affected products