GE recalls CARESCAPE R860 Ventilator

Serious injuries or death may result from the use of these devices. This is a Class I recall, the most serious type of recall.

If your email program has trouble displaying this email, view as a webpage. GE Healthcare Recalls CARESCAPE R860 Ventilator Due to Early Failure of the Backup Batteries that May Cause Unexpected Shut Downs GE Healthcare is recalling CARESCAPE R860 Ventilator due to early failure of the backup batteries, including replacement backup batteries, manufactured on or after April 1, 2019, because the batteries may run out before they are expected to do so. If the ventilator is running on battery power only when the battery fails, ventilation could stop completely, preventing the patient from receiving oxygen and breathing support. The U.S. Food and Drug Administration (FDA) has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries, serious health consequences, or death. Read More Questions? Customers with questions or concerns about this recall should contact GE Healthcare Service at 1-800-437-1171 or the local service representative.

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