Ingenuity TF PET/CT (non-RoHS), Model Number 882456 This device is a diagnostic imaging system...

FDA Recall #Z-0823-2019 — Class II — December 19, 2018

Recall #Z-0823-2019 Date: December 19, 2018 Classification: Class II Status: Terminated

Product Description

Ingenuity TF PET/CT (non-RoHS), Model Number 882456 This device is a diagnostic imaging system that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem produces cross-sectional images of the body by computer reconstruction of x-ray transmission data. The PET subsystem produces images of the distribution of PET radiopharmaceuticals in the patient body (specific radiopharmaceuticals are used for whole body, brain, heart and other organ imaging).

Reason for Recall

A software update is being issued to correct multiple issues identified in the previous software version.

Recalling Firm

Philips Medical Systems (Cleveland) Inc — Cleveland, OH

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

24

Distribution

Worldwide distribution: US (nationwide) to states of: CA, IL, NY, OH, and PA; and to countries of: Australia, Austria, Columbia, Egypt, France, Germany, India, Italy, Lithuania, Netherlands, and Switzerland.

Code Information

Serial Numbers 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2015 2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 2026 2027

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated