Potential exists for one or more axes of the robotic stand to become blocked by their safety brakes; In the event the axis is blocked by its safety brake, the robotic stand can no longer…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Siemens became aware of an issue of incorrect use of the bypass key overriding the built-in collision control creating risk of collision with obstacles or persons when the operator uses the…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Siemens became aware of an issue of incorrect use of the bypass key overriding the built-in collision control creating risk of collision with obstacles or persons when the operator uses the…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
The potential exists for system movement to be permanently blocked by an activation of the collision sensor integrated in the cover of the collimator even when no collision has occurred.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
During a routine inspection of a system, a crack on the C-arm holder was discovered. In the event the C-arm holder has a crack, the stability of the C-arm may be compromised and could lead…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the activation of a collision sensor will cause a block the movement of the floating tabletop and could result in a…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
SOMATOM go.Top (Models #11061640 & 11061648) with software syngo CT VA20A_SP2 and active Guide&GO license No dose documentation and no Dose Alert for the special mode i- Sequence during…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
An error can occur when performing a biopsy using the InSpect function. The acquisition workstation may become unresponsive to normal user interaction, can only take place in rare cases
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
SOMATOM Definition Edge, SOMATOM Definition AS, SOMATOM Definition Flash with software syngo.CT with Software version VA48A_SP5 may result in scanning workflow interruptions and unexpected…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Artis zee/Q systems patient tables may potentially have cracks in the table mainframe, and cause mechanical detachment of the upper part of the patient bed and lead to hazardous situations…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
The action is being initiated due to internal testing which identified a possibility for transducers to exceed the acoustic output power (AOP) values defined . The transit voltage values…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
The action is being initiated due to internal testing which identified a possibility for transducers to exceed the acoustic output power (AOP) values defined . The transit voltage values…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
The action is being initiated due to internal testing which identified a possibility for transducers to exceed the acoustic output power (AOP) values defined . The transit voltage values…
Class IIFDA: OngoingSiemens 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.