FDAFDA · Food and drugs·Recall number Z-0515-2013
MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
Published December 19, 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
A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Distributor
- Nationwide Distribution
- Lot
- Part numbers 7721165, 4787714, 7559375, 10281150, 10281151, 10281152 and 10281183
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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