Reported Sep 4, 2019 · Terminated
Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows
Siemens Medical Solutions USA, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Siemens Medical Solutions USA, Inc · 40 Liberty Blvd · Malvern, PA · 19355-1418
Is this the product you have?
Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows
3 of 3 products
| Model / number | Product as published |
|---|---|
10848280 | Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material Number Artis zee biplane 10094141; Artis Q floor |
10848282 | Artis Q biplane |
10094137 | Artis Q.zen floor 10848353; Artis Q.zen biplane 10848355; Artis zee ceiling |
- Lot codes and dates
- Serial Numbers
123245103302121501148401109589148393111129148400103310148397155235121505109563121506131235121502105125
- Serial Numbers
- Amount recalled
- US 17
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
Why it was recalled
Artis zee/Q systems patient tables may potentially have cracks in the table mainframe, and cause mechanical detachment of the upper part of the patient bed and lead to hazardous situations for patients and medical personnel due to falling parts
This product could cause temporary or reversible health problems — stop using it.
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