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AGFA Corp. recalls IMPAX RIS QDOC 5.8
Recalled February 12, 2014 · FDA recall Z-0919-2014 · AGFA
Hazard
Patient name displayed (printed) on the Patient Report was the wrong patient name. · FDA Class II
Units
14
Sold at
CA, FL, GA, ME, OH, OR, SC, SD, TX and Canada
Description
Patient name displayed (printed) on the Patient Report was the wrong patient name.
Product
IMPAX RIS QDOC 5.8
Manufacturer(s)
AGFA Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →