Pi Pharma Covid-rapid Antigen Test (2020-12-18)
API PHARMA COVID-RAPID ANTIGEN TEST RECALL API Pharma's COVID-Rapid Antigen Test is being recalled across Canada due to issues with the medical device. This is a Class I recall, which means the product could cause serious harm or death. The recall affects COVID-19 rapid antigen tests distributed throughout Canada.
- Reason
- COVID - Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-12-31
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2a179e8b-5ae4-42a4-b237-1a1839d1f56f