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DIGIMED CO., LTD recalls Portable X-ray system
Recalled July 30, 2025 · FDA recall Z-2117-2025 · DIGIMED
Hazard
Some DIOX-602 units currently in use within the United States do not meet the minimum SSD requirement of 18 cm. · FDA Class II
Units
530
Sold at
US
Description
Some DIOX-602 units currently in use within the United States do not meet the minimum SSD requirement of 18 cm.
Product
Portable X-ray system
Manufacturer(s)
DIGIMED CO., LTD
Made in
Korea (the Republic of)
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →