The Recall Desk

FDA (Devices) recall action 79097

Siemens Medical Solutions USA, Inc recalled 3 products on 2018-03-07

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
2018-03-07
Critical
0
Units
—

Why these products were recalled

Potential for liquid entry

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

1–3 of 3

  • HighFDA (Devices)··2018-03-07

    Siemens Axiom Artis Medical Devices Recalled for Liquid Entry Risk

    Siemens Medical Solutions is recalling Axiom Artis devices due to a potential for liquid entry.

    Product
    Axiom Artis, Model Numbers: 5904433, 5904441, 5904649, 5904656, 5917054, 7007755, 7008605, 7412807, 7413078, 7555357, 7555373, 7727717, 7728350 & 7728392
    Category
    Distribution
    0 states
  • ModerateFDA (Devices)··2018-03-07

    Siemens Medical Solutions Recalls Artis Q and Q.Zen Systems

    Siemens Medical Solutions is recalling Artis Q and Q.Zen systems due to a potential for liquid entry.

    Product
    Artis Q and Q.Zen, Model Numbers:10848280, 10848281, 10848282, 10848353 & 10848355
    Category
    Distribution
    0 states