Perimeter Octopus 900 (2019-06-10)

Perimeter Octopus 900 Recall Summary The Perimeter Octopus 900 medical device has been recalled across Canada due to a safety issue. This is a Class I recall, which indicates a serious problem with the device. The recall affects all units of this device that were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-06-21

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/135859d3-20f1-4642-91d1-e0fdf5162c4a