Phadia 250 Instrument (including Software) (2017-11-29)
Phadia 250 Instrument Recall The Phadia 250 Instrument, which includes its software, has been recalled across Canada. This is a Class I recall, which is the most serious type. The specific reason for the recall relates to issues with the medical device itself, though the details of what problem prompted the recall are not specified in this notice.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-01-29
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/15e637c8-e54d-46b5-85ce-b971f1345bb7