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Siemens Medical Solutions USA, Inc recalls Luminos Agile Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studies Mod
Recalled March 1, 2023 · FDA recall Z-1165-2023 · Siemens Medical Solutions USA
Hazard
Potential risk of collision with the ceiling, wall, or objects which may result in serious injury to staff or patients due to room configuration parameters of the system being set to default values · FDA Class II
Units
28 units. Expanded Recall: 506 units
Sold at
US Nationwide distribution.
Description
Potential risk of collision with the ceiling, wall, or objects which may result in serious injury to staff or patients due to room configuration parameters of the system being set to default values
Product
Luminos Agile Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10762472
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →