Health product recall

RAMP Liquid Cardiac Controls Product (2019-03-13)

Starting date:
March 13, 2019
Posting date:
April 29, 2019
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-69712

Last updated: 2019-04-30

Affected Products

RAMP Liquid Cardiac Controls Product

Reason

Recall of RAMP Liquid Cardiac Controls product for in vitro diagnostic use in the quality control of cardiac marker tests - field correction for product deficiency.

Affected products

RAMP Liquid Cardiac Controls Product

Lot or serial number

070318

Model or catalog number

C2003-2

Companies
Manufacturer

Response Biomedical Corporation

1781 – 75th Avenue W

Vancouver

V6P 6P2

British Columbia

CANADA