This page has been archived on the Web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

Aquios Cl Flow Cytometry System

Starting date:
August 21, 2017
Posting date:
September 11, 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-64476

Reason

An erroneous configuration setting during servicing may be possible on the Aquios CL instruments. If the incorrect configuration occurs, the probe may aspirate samples only from a single tube and will not aspirate from the remaining tubes in the cassette.

Affected products

Aquios Cl Flow Cytometry System

Lot or serial number

  • AY03004
  • AY25038
  • AZ12027
  • BA05016

Model or catalog number

B30166

Companies

Manufacturer
Beckman Coulter Inc.
250 S. Kraemer Blvd.
Brea
92821
UNITED STATES