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ImmunoCAP Specific IgE Control H (2016-01-28)
- Starting date:
- January 28, 2016
- Posting date:
- February 12, 2016
- 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-57122
Affected Products
- Phadia 100 System - Specific IgE Assay
- Phadia 250 System - Specific IgE Assay
Affected products
A. Phadia 100 System - Specific IgE Assay
Lot or serial number
- H9FN
- HARB
Model or catalog number
10-9530-01
Companies
- Manufacturer
-
PHADIA AB
RAPSGATAN 7
UPPSALA
SWEDEN
B. Phadia 250 System - Specific IgE Assay
Lot or serial number
- H9FN
- HARB
Model or catalog number
10-9530-01
Companies
- Manufacturer
-
PHADIA AB
RAPSGATAN 7
UPPSALA
SWEDEN