Patient Data Module (pdm) (2020-05-21)

Recall Summary The Patient Data Module (PDM) is being recalled due to a medical device issue. This recall applies to PDM devices distributed across Canada. This is classified as a Class I recall, which is the most serious type.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-06-12
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b53dea3e-91f7-44c9-9248-24c679dc69c8