This page has been archived on the Web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

Hemolung RAS Cartridge Kit (2013-11-26)

Starting date:
November 26, 2013
Posting date:
February 10, 2014
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-37843

Recalled Products

Hemolung RAS Cartridge Kit

Reason

Alung technologies Inc. has identified a manufacturing defect in a limited number of Hemolung cartridges (a component of Hemolung cartridge kit) which may result in unexpected failure of the device, cessation of therapy and a visible and audible controller alarm.

Affected products

Hemolung RAS Cartridge Kit

Lot or serial number

Serial numbers:

010556

010557

010559

010560

010561

010602

Model or catalog number

10000

Companies
Manufacturer

Alung Technologies

2500 Jane Street, Suite 1

Pittsburgh

15203-2216

Pennsylvania

UNITED STATES