Phadia 100/250 System (2016-04-21)
PHADIA 100/250 System Recall Summary The PHADIA 100/250 System, a medical laboratory device used for allergy and immunology testing, is being recalled across Canada. The recall is classified as Class I, the most serious type, due to issues with the medical device itself. This recall affects healthcare facilities and laboratories that use this equipment for patient testing.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-05-20
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/19a7666e-ee98-40df-b9d7-8947cb122f19