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