EPIQ 5 and EPIQ 7 Ultrasound Systems, Diagnostic Ultrasound System (2019-05-01)
- Starting date:
- May 1, 2019
- Posting date:
- May 10, 2019
- 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-69898
Last updated: 2019-05-10
Affected Products
A. EPIQ 5 Ultrasound System
B. EPIQ 7 Ultrasound System
C. Diagnostic Ultrasound System
Reason
When the user uses the edit functionality on the patient data entry (PDE) screen, there is the potential that one patient's images could get unexpectedly moved into another patient's folder.
Affected products
A. EPIQ 5 Ultrasound System
Lot or serial number
Not applicable.
Model or catalog number
EPIQ 5
Companies
- Manufacturer
-
Philips Ultrasound Inc.
22100 Bothell-Everett Highway
Bothell
98021-8431
Washington
UNITED STATES
B. EPIQ 7 Ultrasound System
Lot or serial number
Not applicable.
Model or catalog number
EPIQ 7
Companies
- Manufacturer
-
Philips Ultrasound Inc.
22100 Bothell-Everett Highway
Bothell
98021-8431
Washington
UNITED STATES
C. Diagnostic Ultrasound System
Lot or serial number
Not applicable.
Model or catalog number
AFFINITI 70
Companies
- Manufacturer
-
Philips Ultrasound Inc.
22100 Bothell-Everett Highway
Bothell
98021-8431
Washington
UNITED STATES