Reported Aug 12, 2015 · Terminated

Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and…

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 · 51 Valley Stream Pkwy · Malvern, PA · 19355-1406

Is this the product you have?

  • Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography, general angiography, rotational angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures.
Lot codes and dates
  • Model Number of device
    • 10094141
    • 10094143
    • 10094137
    • 10094135
    • 10094142
    • 10848280
    • 10280959
    • 10848283
    • 10848353
  • serial numbers

    1,271 of 1,271 codes

    • 146669
    • 153131
    • 153229
    • 160851
    • 146877
    • 146996
    • 146663
    • 147100
    • 124002
    • 147049
    • 147678
    • 146406
    • 146407
    • 146411
    • 136077
    • 154502
    • 135746
    • 153172
    • 153315
    • 153317
    • 153318
    • 160879
    • 146121
    • 146710
    • 137165
    • 146945
    • 147084
    • 153992
    • 147189
    • 147190
    • 153335
    • 153695
    • 135120
    • 135322
    • 146679
    • 153101
    • 153102
    • 146232
    • 147573
    • 154616
    • 153727
    • 146408
    • 146409
    • 146728
    • 146335
    • 146659
    • 153779
    • 146993
    • 137226
    • 153280
    • 153648
    • 153674
    • 160395
    • 146898
    • 153166
    • 154536
    • 146965
    • 160484
    • 135757
    • 136513
Amount recalled
N/A

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate the components inside the table. If this occurs, table movements may no longer be possible. No injuries reported.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 7, 2016 · Data as of Sep 19, 4:47 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.