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Siemens AG/Siemens Healthcare GmbH FDA Recalls

3 recalls on file across devices, 0 of them Class I and 3 still open. Matched by name to SIEGY.

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Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product
ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventionaClass IIJun 26, 2024A potential issue with ARTIS icono systems equipped with a s
ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventionaClass IIJun 26, 2024A potential issue with ARTIS icono systems equipped with a s
ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventionaClass IIJun 26, 2024A potential issue with ARTIS icono systems equipped with a s

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