ClearanceBrief
Recall Z-1578-2009 ยท JAK System, X-Ray, Tomography, Computed

Philips Medical Systems (Cleveland) Inc

TumorLoc software application, Software Versions: 23.1.1, 20.7.13, and 20.8.15 for use on the GEMINI TF 16 and GEMINI TF 64 Slice PET/CT Systems, Catalog Numbers: 882470 - GEMINI TF 16 Slice; 882471 - GEMINI TF 64 Slice; and 882473 - GEMINI TF 16 Slice Base Configuration. Model Numbers: 4535 679 83931 - GEMINI TF 16 Slice; 4535 679 94741 - GEMINI TF-64 Slice and 4535 674 41711 - GEMINI TF 16 Slic

DateJul 6, 2009 (initiated Feb 19, 2009)
StatusTerminated
ReasonA software anomaly in the TumorLoc software for the firm's Brilliance CT scanners was discovered. The same software anomaly was subsequently determined to be present in the firm's GEMINI PET/CT units. The software defect results in a the potential for data to be lost during reconstruction of images in which slices can either be discarded, or interleaved based upon their series ID.
Root causeSoftware design
ActionAn "URGENT - Field Safety Notice" dated February 12, 2009 was sent via FedEx to domestic customers. The notice described the affected products, issue, involved hazard should problem occur and corrective actions for the customer/user. The letter also notified users/customers that a Philips Healthcare Field Service Engineer will contact and visit their site within 6 months to install a TumorLoc upgrade. Notification will also be sent to the international consignees by Philips personnel. For further information or support concerning this issue, please contact your local Philips representative
Quantity13 units
DistributionWorldwide Distribution -- US, Columbia, Germany, France, Netherlands, Canada, Belgium and Slovenia.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K033326PHILIPS PLUS COMPUTED TOMOGRAPHY SYSTEM
Philips Medical Systems, Inc., Oct 29, 2003