This page has been archived on the Web

Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.

Health product recall

Avea Ventilator (2016-05-17)

Starting date:
May 17, 2016
Posting date:
June 13, 2016
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-58852

Affected products

A. Avea Ventilator

Reason

Incorrectly installed F1 fuse on the AVEA Ventilator TCA Board may result in a failed/blown fuse, causing loss of power to the UIM

Affected products

A. Avea Ventilator

Lot or serial number

All lots

Model or catalog number

AVEA

Companies
Manufacturer
Carefusion
22745 Savi Ranch Parkway
Yorba Linda
92887
California
UNITED STATES