Herbst Bite Jumper (2018-06-07)

Herbst Bite Jumper Recall Summary The Herbst Bite Jumper, a medical device used in orthodontic treatment, is being recalled across Canada due to safety concerns. The device was distributed throughout Canada and has been classified as a Class I recall, indicating a serious issue. This recall affects any Herbst Bite Jumper devices that were in use or in stock during the recall period.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-02-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1c84c30f-0bfe-40af-8e40-a06c8da23a9b