FDAFDA · Food and drugs·Recall number Z-0195-2019
Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.
Published October 24, 2018 · Recall initiated: August 30, 2018
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
Remote comparison studies displayed may be associated with the wrong patient, without a caution icon present.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- GE Healthcare, LLC
- Distributor
- NY
- Lot
- SYSTEM ID: 315470CPUWPV UDI #: 8406821038 00DE #: 2090255-001
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.