PlainRecalls
FDA Devices Moderate Class II Ongoing

Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.

Reported: February 14, 2024 Initiated: December 13, 2023 #Z-1055-2024

Product Description

Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.

Reason for Recall

A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.

Details

Recalling Firm
PHILIPS MEDICAL SYSTEMS
Units Affected
US: 33, OUS 177
Distribution
Worldwide - US Nationwide distribution in the states of AR, AZ, GA, HI, IN, KY, MA, MD, MN, NY, OH, PA, TX & WV; the countries of Australia, Austria, Belgium, China, Czech Republic, Denmark, Germany, Israel, Italy, Japan, Macao, Malaysia, Netherlands, Norway, Palestine, Panama, Portugal, Singapore, South Korea, Spain, Switzerland, Taiwan, Thailand & United Kingdom.
Location
Cambridge, MA

Frequently Asked Questions

What product was recalled?
Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.. Recalled by PHILIPS MEDICAL SYSTEMS. Units affected: US: 33, OUS 177.
Why was this product recalled?
A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 14, 2024. Severity: Moderate. Recall number: Z-1055-2024.