The Recall Desk

FDA (Devices) recall action 71711

Siemens Medical Solutions USA, Inc recalled 3 products on 2015-08-12

The FDA (Devices) publishes a recall like this one as 3 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 3 pages.

Products
3
Announced
2015-08-12
Critical
0
Units
—

Why these products were recalled

The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate the components inside the table. If this occurs, table movements may no longer be possible. No injuries reported.

The agency’s own wording, quoted from the enforcement report.

1–3 of 3

  • HighFDA (Devices)··2015-08-12

    Siemens Axiom Artis Angiography Systems Recalled for Liquid Seepage Risk

    Siemens Medical Solutions is recalling Axiom Artis angiography systems because liquid may seep through the top cover and penetrate internal components, potentially disabling table movements.

    Product
    Axiom Artis systems, dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography, gene
    Category
    Distribution
    0 states
  • HighFDA (Devices)··2015-08-12

    Siemens Artis zee Systems Recalled for Potential Liquid Seepage

    Siemens Medical Solutions is recalling Artis zee angiography systems because liquid may seep through the table cover, potentially preventing table movement.

    Product
    Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiograph
    Category
    Distribution
    0 states
  • ModerateFDA (Devices)··2015-08-12

    Siemens Artis Q Systems Recalled for Potential Liquid Ingress

    Siemens Medical Solutions is recalling Artis Q angiography systems because liquid may seep through the top cover, potentially disabling table movements. No injuries have been reported.

    Product
    Artis Q systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography, general
    Category
    Distribution
    0 states