United StatesLUMINOS Lotus Max (Model 11574100) and Luminos dRF Max (Model 10762471) systems running software version VF11, equipped with a bucky wall stand for mobile detectors and without a ceiling stand, are affected. They were recalled because when switching quickly between organ programs (OGPs) the collimation may be incorrect.
What's being recalled
LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471
Recalling firm: Siemens Medical Solutions USA, Inc, Malvern, PA, United States.
How to identify it
(01)04056869269931(21)10330
The hazard
A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When switching quickly between organ programs (OGPs) the collimation may be incorrect.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
U.S. and OUS
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)