This page has been archived on the Web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

IQ Body Fluid Controls

Starting date:
May 30, 2017
Posting date:
June 13, 2017
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-63622

Reason

The expiration dates listed on the IQ body fluid controls - Level I and Level II package labeling (vial, assay sheet and kit box) do not correspond to the expiration date displayed by the IQ200 analyzer.

Affected products

IQ Body Fluid Controls

Lot or serial number

  • KIT LOT 6340
  • KIT LOT 7030
  • KIT LOT 7086

Model or catalog number

800-3219

Companies

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