Heartstart Hs1 Home, Hs1 Onsite, Frx Or Fr2/fr2+ Aed (2021-03-03)

Recall Summary Philips is recalling certain HeartStart automated external defibrillators (AED) models—HS1 Home, HS1 OnSite, FRx, and FR2/FR2+—due to a medical device issue. These devices were distributed across Canada. This is a Class I recall, which indicates a serious safety concern.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-03-18

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/68a03b52-9560-426e-86e6-d0b3254e3ac6