FDA Enforcement Class II Terminated

GEMINI TF 16 Slice CT/PET System. The Philips GEMINI PET/CT Imaging Systems are a family of integrated diagnostic X-ray Computed Tomography (CT) and Positron Emission Tomography (PET) systems suitable for a wide range of diagnostic applications.

Recall: Z-2195-2015 · Reported July 29, 2015

Enforcement

Recall Number
Z-2195-2015
Event ID
71699
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Philips Medical Systems (Cleveland) Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 29, 2015
Initiation Date
July 1, 2015
Classification Date
July 22, 2015
Termination Date
June 26, 2018
Address
595 Miner Rd, N/A, Cleveland, OH, 44143-2131, United States

Description

GEMINI TF 16 Slice CT/PET System. The Philips GEMINI PET/CT Imaging Systems are a family of integrated diagnostic X-ray Computed Tomography (CT) and Positron Emission Tomography (PET) systems suitable for a wide range of diagnostic applications.

Reason

Philips has identified four (4) software defects in the Tumor LOC software application that may potentially result in irradiation of healthy tissue or non-irradiation of diseased tissue.

Code Info

Model #882470 GEMINI TF 16 Slice (453567983931); Serial Number: 7052, 7060, 7093, 7096, 7121, 7123, 7128, 7129, 7185, 7187, 7220, 7226 & 7570.

Distribution

Worldwide Distribution - US Nationwide, Australia, Belgium, Brazil, Canada, China, Denmark, France, Germany, Israel, Italy, Japan, Lebanon, Netherlands, Portugal, Saudi Arabia, South Africa, Switzerland, Thailand, Venezuela & Vietnam.

Quantity

13 Units