Z-0309-2019 Class II Terminated
FDA device recall Z-0309-2019 was initiated by Philips Medical Systems (Cleveland) Inc on June 7, 2017 and is designated Class II. Reason for recall: It was reported that scanners running certain software versions provide confusing information in the "Impressions" section of the Calcium Score report. The generated report provides multiple analyse… The recall status is terminated (terminated July 3, 2019). Affected quantity: 1890.
Recall Details
- Product Type
- Devices
- Report Date
- November 7, 2018
- Initiation Date
- June 7, 2017
- Termination Date
- July 3, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1890
Product Description
Ingenuity Core (Model No. 728321), Software version 4.1.6 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories.
Reason for Recall
It was reported that scanners running certain software versions provide confusing information in the "Impressions" section of the Calcium Score report. The generated report provides multiple analyses of the amount of plaque detected, as if they all apply to the patient at the same time. This misleading guidance can be potentially misleading to the user, and may lead to mistreatment of the patient.
Distribution Pattern
US Nationwide Distribution
Code Information
software versions 4.1.6