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Siemens Medical Solutions USA, Inc recalls Siemens Artis Q floor --Interventional Fluoroscopic X-Ray System Model Number: 10848280
Recalled July 10, 2019 · FDA recall Z-1898-2019 · Siemens Medical Solutions USA
Hazard
Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel · FDA Class II
Units
12
Sold at
Nationwide
Description
Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel
Product
Siemens Artis Q floor --Interventional Fluoroscopic X-Ray System Model Number: 10848280
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →