Ih-1000 (2018-03-13)

Recall Summary The IH-1000 medical device has been recalled across Canada due to a safety concern classified as Class I, which indicates a serious risk to health. The recall was issued on March 13, 2018, and affects all units distributed throughout Canada. Specific details about the device's intended use and the particular safety issue are not provided in this notice.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-04-06

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6a4b051a-41fa-4179-a41d-da095f056fbf