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iCAD Recalls
1 recall on record · March 11, 2015 to March 11, 2015 · Medical Devices
March 11, 2015
Medical Devices
FDA
iCAD, Inc. recalls DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2
Hazard: A device malfunction may cause the biopsy needle to fail to reach the intended target. If location confirming radiographs are not taken and properly evaluated, biopsy site mislocation can result in non-target tissue being sampled rather than target tissue. May result in an incorrect diagnosis.
iCAD Recalls | RecallWatchUSA