LOGIC 9 and LOGIQ E9 General Purpose Ultrasound System (2018-03-28)
- Starting date:
- March 28, 2018
- Posting date:
- April 24, 2018
- 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-66536
Affected products
- LOGIQ 9 Ultrasound System
- LOGIQ E9 General Purpose Ultrasound System
Reason
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock. This can lead to injuries up to and including cardiac arrhythmia or cardiac arrest. A minor injury has been reported as a result of this issue.
Affected products
-
LOGIQ 9 Ultrasound System
Lot or serial number
Not applicable
Model or catalog number
H4905SM/SR
Companies
- Manufacturer
-
GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
9900 Innovation Drive
Wauwatosa
53226
Wisconsin
UNITED STATES
B. LOGIQ E9 General Purpose Ultrasound System
Lot or serial number
Not applicable
Model or catalog number
5205000-7
5205000-9
Companies
- Manufacturer
-
GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
9900 Innovation Drive
Wauwatosa
53226
Wisconsin
UNITED STATES