Fidji (2016-09-27)

FIDJI Recall Summary Fidji is a medical device that was recalled across Canada due to safety or effectiveness concerns classified as Class I, the most serious type of recall. The specific details about what the product is used for and the exact nature of the problem are not provided in the available information.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-11-15

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8fbbe07c-55e5-4502-a4be-2d37ad7987b7