Carescape R860 (2018-10-04)

Carescape R860 Recall Summary GE Healthcare's Carescape R860 ventilator is being recalled in Canada due to a defect in how it handles certain alarm conditions during patient ventilation. The device may fail to properly alert clinicians to serious breathing problems, potentially delaying treatment. The recall affects Carescape R860 ventilators distributed across Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-10-26
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e738e484-dc4e-4807-a9e6-37129a90d2c0