A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. This may cause a delay in diagnosis or patient scans.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need for patient rescan.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need for patient rescan.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. This may cause a delay in diagnosis or patient scans.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. This may cause a delay in diagnosis or patient scans.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Siemens Medical Solutions USA, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.