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Health product recall

Arkon Anesthesia System

Starting date:
February 17, 2017
Posting date:
March 16, 2017
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-62634

Reason

Spacelabs has received reports of the failure of the power supply that provides electricity to the Arkon Subsystems. This failure causes the system to run on its internal battery(s) without charging them or providing the user the "on battery" display messages. Once the batteries reach their minimal charge level, the Arkon powers down and the backup audible buzzer alarm activates.

Affected products

Arkon Anesthesia System

Lot or serial number

ARKN-000005
ARKN-000015

Model or catalog number

ARKON

Companies

Manufacturer
Spacelabs Healthcare Inc.
35301 SE Center Street
Snoqualmie
98065
Washington
UNITED STATES