Health product recall

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

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

Carescape One

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number
  • 2078006-001
Companies
Manufacturer

GE Medical Systems Information Technologies, Inc.

8200 W Tower Ave

Milwaukee

53223

Wisconsin

UNITED STATES