FDAFDA · Food and drugs·Recall number Z-0919-2014
IMPAX RIS QDOC 5.8
Published February 12, 2014 · Recall initiated: January 8, 2014
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
Patient name displayed (printed) on the Patient Report was the wrong patient name.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- AGFA Corp.
- Distributor
- CA, FL, GA, ME, OH, OR, SC, SD, TX and Canada
- Lot
- Software IMPAX RIS 58 and higher
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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