EPIQ DIAGNOSTIC ULTRASOUND SYSTEM (2021-09-20)
- Starting date:
- September 20, 2021
- Posting date:
- October 8, 2021
- 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-76603
Last updated:
2021-10-08
Affected Products
EPIQ DIAGNOSTIC ULTRASOUND SYSTEM
Reason
Philips has become aware of a software issue that can potentially cause the EPIQ CVXI system to issue an error notification and become unresponsive during clinical use.
Affected products
EPIQ DIAGNOSTIC ULTRASOUND SYSTEM
Lot or serial number
Not applicable.
Model or catalog number
EPIQ
Companies
- Manufacturer
-
PHILIPS ULTRASOUND, INC.
22100 BOTHELL-EVERETT HIGHWAY, BOTHELL
BOTHELL
Washington
UNITED STATES