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SEDECAL SA recalls Phoenix mKDR, digital mobile diagnostic x-ray system
Recalled March 8, 2023 · FDA recall Z-1202-2023 · SEDECAL SA
Hazard
Sedecal was informed of 3 incidents of erratic movements related to X-ray mobile systems. · FDA Class II
Units
53 units
Sold at
US, Argentina, Panama
Description
Sedecal was informed of 3 incidents of erratic movements related to X-ray mobile systems.
Product
Phoenix mKDR, digital mobile diagnostic x-ray system
Manufacturer(s)
SEDECAL SA
Made in
Spain
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →