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AGFA Healthcare Corp. recalls Agfa Digital Radiography X-Ray System DX-D 100 Product Usage: Is indicated for use in providing diagnostic quality i
Recalled August 20, 2014 · FDA recall Z-2176-2014 · AGFA Healthcare
Hazard
Unit was mislabeled with a factory label showing 32 KW output power. · FDA Class III
Units
1
Sold at
US in the state of WV
Description
Unit was mislabeled with a factory label showing 32 KW output power.
Product
Agfa Digital Radiography X-Ray System DX-D 100 Product Usage: Is indicated for use in providing diagnostic quality images to aid the physician with diagnoses.
Manufacturer(s)
AGFA Healthcare Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →