Siemens Artis zee/zeego X-Ray Systems Recalled for Cooling System Leak
Siemens is recalling 1,757 Artis zee/zeego angiographic X-ray systems because a possible leak in the cooling system could allow fluids to seep into the equipment cabinet.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text describes a potential fluid leak without reporting any injuries, illnesses, or deaths, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Siemens Medical Solutions USA, Inc. is recalling 1,757 Artis zee/zeego angiographic X-ray systems. These systems are used for single and biplane diagnostic imaging and interventional procedures, including cardiac and neuro angiography, general and rotational angiography, operating room angiography, multipurpose angiography, and whole body radiographic/fluoroscopic procedures.
The recall is due to a possible leak in the cooling system. This leak can occur sporadically in affected systems, and fluids could potentially seep into the equipment cabinet. The affected model numbers are 5917054, 7008605, 7412807, 7413078, 7555357, 7555365, 7555373, 7727717, 7728392, 10094135, 10094137, 10094139, 10094141, 10094142, 10094143, and 10280959.
The affected systems were distributed nationwide to all 50 states, the District of Columbia, and Puerto Rico. Healthcare facilities should contact Siemens Medical Solutions USA, Inc. for further instructions regarding the recall and necessary corrective actions.
The recalled product
- Product
- Artis zee/zeego (system, x-ray, angiographic) for single and biplane diagnostic imaging and interventional procedures such as cardiac and neuro angiography, general and rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoro
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Hazard
- Affected units
- 1,757
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (16)
- Model Numbers: 5917054
- 7008605
- 7412807
- 7413078
- 7555357
- 7555365
- 7555373
- 7727717
- 7728392
- 10094135
- 10094137
- 10094139
- 10094141
- 10094142
- 10094143
- 10280959
Distribution
Part of a larger recall action
This product is one of 2 recalled by Siemens Medical Solutions USA, Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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