to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Error introduced into PET images acquired and reconstructed with VJ20A software. Array values are indexed improperly when the norm file is created during QC. During data reconstruction,…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms.…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
A software functionality in the report sections Findings Information and Summary of Measured Findings is not performing properly. The system will use the original values instead of…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
When the archiving configuration is changed, data received/created after the upgrade may be flagged as "Not to be archived". This is caused by the automatic function for cleaning up…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Certain patient table systems may have a missing or incorrectly installed snap ring that could cause the bolt to slide out of its base and the tabletop carriage to slide to the floor.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Certain systems may have leaking of the plastic coolant couplings, the liquid can enter into the flat panel detector leading to a failure of the detector. It may be necessary to cancel or…
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.