Carescape One (2020-04-13)

Starting date:

April 13, 2020

Posting date:

May 1, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-72945

Last updated: 2020-05-01

• Reason
• Affected products

Affected Products

Carescape One

Reason

ECG parameter and waveform data may be lost when used in conjunction with an automated external defibrillator (AED) or any AED capable defibrillator when used in AED mode

Affected products