This page has been archived on the Web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.
Advanced Perfusion System 1 - Base Unit (2013-04-23)
- Starting date:
- April 23, 2013
- Posting date:
- May 8, 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-39403
Recalled Products
Advanced Perfusion System 1 - Base Unit
Reason
System malfunction caused by an inadequate crimp quality on internal cables creating loss or fluctuation of internal power on one side of the system's base.
Affected products
Advanced Perfusion System 1 - Base Unit
Lot or serial number
0011-1137
Model or catalog number
801763
Companies
- Manufacturer
-
Terumo Cardiovascular Systems Corp.
6200 Jackson Road
Ann Arbor
48103
Michigan
UNITED STATES