FDAFDA · Food and drugs·Recall number Z-2620-2017
Merge OrthoPACS software.
Published June 28, 2017 · Recall initiated: May 24, 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
A migrated study that has annotations will display the annotations, but when a prior study is loaded that should have annotations, the second study will not display annotations.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Merge Healthcare, Inc.
- Distributor
- Distribution was made nationwide to medical facilities. There was no foreign/government/military distribution.
- Lot
- Versions 6.6, 6.6.1, and 6.6.2
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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