ClearanceBrief
Recall Z-0461-2008 ยท KPS System, Tomography, Computed, Emission

Philips Medical Systems (Cleveland) Inc

Philips Medical Systems, GEMINI TF 16 & 64 slice PET/CT Systems, diagnostic imaging systems for fixed or mobile installations that combine Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems, Philips Medical Systems, Cleveland, OH 44143

DateJan 31, 2008 (initiated Sep 21, 2007)
StatusTerminated
ReasonArtifacts: Artifacts may appear in some images from head scans on the CT subsystem of the GEMINI PET/CT system. Reading images with these artifacts may lead to misdiagnosis or improper treatment.
Root causeSoftware design
ActionPhilips Medical notified domestic customers via Product Safety Notification dated May 30, 2007. The product safety notification includes a Technical Bulletin notifying customers of the issue and how to avoid it. This information will be used until the software correction becomes available. The software correction will be released in October 2008. Once software is available, the firm will begin correcting the field.
Quantity61
DistributionWorldwide Distribution - USA, Australia, Belgium, Canada, China, Denmark, England, Finland, France, Germany, Hong Kong, Hungary, India, Ireland, Italy, Japan, Jordan, Korea, Netherlands, Poland, Portugal, Saudi Arabia, Slovenia, Spain, Sweden, Taiwan, Turkey, and Venezuela.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K051170GEMINI GXL
Philips Medical Systems (Cleveland), Inc., May 23, 2005
K052640GEMINI RAPTOR
Philips Medical Systems (Cleveland), Inc., Oct 7, 2005