Lifepak 20e Defibrillator/monitor (2017-12-07)

Recall Summary The LIFEPAK 20e defibrillator/monitor devices are being recalled across Canada due to a medical device issue. This recall affects users of this specific defibrillator model that was distributed throughout Canada. The recall is classified as Class I, which is the most serious type of recall.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-01-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/96569ac0-0e84-4e8c-ada1-76c4e74dbf25