Siemens Artis Zee and Zeego Medical Devices Recalled for Liquid Entry Risk
Siemens Medical Solutions is recalling Artis Zee and Zeego devices due to a potential for liquid entry.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (medical device) where injury has not yet been reported, fitting the criteria for a High severity score.
Plain-English summary
Siemens Medical Solutions USA, Inc. is recalling Artis Zee and Zeego medical devices, including specific model numbers such as 10094135, 10094137, and 10094141. The recall is issued because of a potential for liquid entry into the devices.
The affected products were distributed nationwide in the United States. The source text does not specify the exact number of units recalled or the specific dates of distribution.
Consumers and healthcare facilities should contact Siemens Medical Solutions USA, Inc. for further instructions on how to manage the recalled devices.
The recalled product
- Product
- Artis Zee and Zeego, Model Numbers: 10094135, 10094137, 10094141, 10094142, 10094143, 10280959, 10848283 & 10848354
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Hazard
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 (20)
- 10094135
- 10094137
- 10094141
- 10094142
- 10094143
- 10280959
- 10848280
- 10848281
- 10848282
- 10848353
- 10848354
- 10848355
- 5904433
- 5904441
- 5904649
- 5904656
- 5917054
- 7007755
- 7008605
- 7412807
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 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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