Is4000 (erbe Footswitch) (2019-02-26)

Recall Summary The IS4000 Erbe Footswitch, a medical device distributed across Canada, has been recalled due to safety concerns classified as Class I (the most serious type). The specific hazard and affected patient population are not detailed in the information provided.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-03-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8aa255dc-292d-4869-a5d3-d32fff94c125