International safety notice
Safety Notice concerning Brilliance CT Big Bore having TumorLOC in versions prior 3.6, GEMINI TF 16 and 64 Slice, GEMINI TF Big Bore, GEMINI LXL PET/CT Systems and Extended Brilliance Workspace with TumorLOC, Philips Healthcare
Germany / BfArM · DEU · Nov 26, 2012
Key facts
| Title | Safety Notice concerning Brilliance CT Big Bore having TumorLOC in versions prior 3.6, GEMINI TF 16 and 64 Slice, GEMINI TF Big Bore, GEMINI LXL PET/CT Systems and Extended Brilliance Workspace with TumorLOC, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Safety Notice concerning Brilliance CT Big Bore having TumorLOC in versions prior 3.6, GEMINI TF 16 and 64 Slice, GEMINI TF Big Bore, GEMINI LXL PET/CT Systems and Extended Brilliance Workspace with TumorLOC, Philips Healthcare |
| Manufacturer | Safety Notice concerning Brilliance CT Big Bore having TumorLOC in versions prior 3.6, GEMINI TF 16 and 64 Slice, GEMINI TF Big Bore, GEMINI LXL PET/CT Systems and Extended Brilliance Workspace with TumorLOC, Philips Healthcare |
| Models | 11096, 11861, 10348, 11724, 10402, 10705, 11693, 11597, 10331, 728243, 75000, 10487 and 31 more |
| Date | Nov 26, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1