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FDA (Device enforcement)Recalled 2023-10-17class ii

Siemens Medical Solutions USA, Inc: ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100

Hazard

Potential hardware issue for ARTIS icono ceiling system: collision sensor may falsely signal non-existing collisions for up to half an hour when the system is switched off for a longer time (e.g., overnight) and switched on. During this time, system movement is only possible with the "override" function with very slow speed and without further collision protection. This may lead to temporary unavailability of the system for diagnostic and therapeutic usage.

Details from the source

Reason for recall: Potential hardware issue for ARTIS icono ceiling system: collision sensor may falsely signal non-existing collisions for up to half an hour when the system is switched off for a longer time (e.g., overnight) and switched on. During this time, system movement is only possible with the "override" function with very slow speed and without further collision protection. This may lead to temporary unavailability of the system for diagnostic and therapeutic usage. Distribution: US Nationwide - Worldwide Distribution: Domestic distribution to FL GA IA IL IN MI MN MO MT PA TX. Foreign distribution to Australia Canada Switzerland China Germany Denmark Egypt Spain Finland United Kingdom Israel Netherlands Sweden South Africa Quantity: 38 worldwide, 11 US Lot/code info: UDI-DI 04056869295923 Serial Numbers: All SN's associated with material number 11328100

UPC codes

04056869295923

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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