Reported Feb 12, 2014 · Terminated
IMPAX RIS QDOC 5.8
AGFA Corp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: AGFA Corp. · 10 S Academy St · Greenville, SC · 29601-2632
Is this the product you have?
- IMPAX RIS QDOC 5.8
- Lot codes and dates
- Software IMPAX RIS 58 and higher
- Amount recalled
- 14
Where it was sold
Why it was recalled
Patient name displayed (printed) on the Patient Report was the wrong patient name.
This product could cause temporary or reversible health problems — stop using it.
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