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SALMONELLA AGGLUTINATING SERUM O 23 (2015-11-03)
- Starting date:
- November 3, 2015
- 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-55868
Affected Products
SALMONELLA AGGLUTINATING SERUM O 23
Reason
Product (serum) is failing to detect positive O 23 strains.
Affected products
SALMONELLA AGGLUTINATING SERUM O 23
Lot or serial number
1260
Model or catalog number
PL.6025
Companies
- Manufacturer
-
Pro-Lab Diagnostics
3 Bassendale Road
Bromborough, Merseyside
CH62 3QL
UNITED KINGDOM