Defibrillation Pads (2016-01-27)

Defibrillation Pads Recall Summary Defibrillation pads have been recalled across Canada due to a defect classified as a Class I safety issue (the most serious category). The pads are medical devices used with defibrillators to deliver electrical therapy to patients experiencing certain heart rhythms. The specific reason for the recall relates to a problem with the device itself, though the details of what defect was identified are not provided in this notice.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-02-22

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5cf628fc-d0fe-46ff-839e-25718fb693f9