Philips Omnidiagnost And Omnidiagnost Eleva (2018-05-07)

Philips OmniDiagnost and OmniDiagnost Eleva Recall Philips is recalling OmniDiagnost and OmniDiagnost Eleva X-ray systems distributed across Canada due to a medical device issue. This is a Class I recall, the most serious classification. The affected devices were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-05-18
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/121d905c-7626-4206-b1f5-6abea1eb58b8