API PHARMA COVID-RAPID ANTIGEN TEST (2020-12-18)
- Starting date:
- December 18, 2020
- Posting date:
- December 31, 2020
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-74685
Last updated:
2020-12-31
Affected Products
API PHARMA COVID-RAPID ANTIGEN TEST
Reason
Samples sent to Canada for study use prior to Health Canada authorization.
Affected products
API PHARMA COVID-RAPID ANTIGEN TEST
Lot or serial number
All lots.
Model or catalog number
Not applicable.
Companies
- Manufacturer
-
API PHARMA USA LLC
1521 ALTON ROAD, SUITE 369
MIAMI BEACH
33139
Florida
UNITED STATES