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Elekta, Inc. recalls DMLC IV-ERGO - Beam shaping block for Radiation Therapy.
Recalled September 11, 2013 · FDA recall Z-2157-2013 · Elekta
Hazard
Clinical mistreatment may occur when there are errors in the clinical workflow, or settings are incorrect. · FDA Class II
Units
31
Sold at
Nationwide distribution: AL, CT, FL, GA, IA, MS, MO, NJ, NY, ND, OH, OK, PA, RI, TX, VA and Puerto Rico.
Description
Clinical mistreatment may occur when there are errors in the clinical workflow, or settings are incorrect.
Product
DMLC IV-ERGO - Beam shaping block for Radiation Therapy.
Manufacturer(s)
Elekta, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →