FDAFDA · Food and drugs·Recall number Z-1491-2017
ONCOR" Expression ONCOR" Impression ONCOR" Impression plus
Published March 29, 2017 · Recall initiated: February 14, 2017
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
Software update
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Distributor
- Distributed throughout the United States
- Lot
- Device Model# 7360717, 5857920, 5857912
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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