FDAFDA · Food and drugs·Recall number Z-0480-2013
Siemens Mobilette Mira, intended use as Mobile x-ray system.
Published December 12, 2012 · Recall initiated: October 10, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
There is a risk of lost images during examination.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Distributor
- Nationwide distribution: USA including states of: GA, ID, IL, IA, NE, NC, OH, SD, TX, and WI.
- Lot
- Model Number 10273100
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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