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Recall Observatory FDA recall evidence

Device product

Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of 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 with the AXIOM Artis zee and Q/ Q.zen family include cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. AXIOM Artis zee and Q/ Q.zen can also support the acquisition of position triggered imaging for spatial data synthesis.

Z-1339-2019

April 09, 2019

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 82730
Status
Terminated
Classification
Class II
Quantity
459 (116 US)
Official record key
device-enforcement:Z-1339-2019

Official wording

Reason: In affected Artis systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement.

Code information: Serial Numbers 138260 138221 138259 138250 138268 138266 124286 125245 148402 148401 148384 148390 147249 148393 148411 148400 148358 148361 148397 148392 148382 148363 148375 155237 155203 155226 155227 155235 131235

Distribution pattern: Worldwide distribution - US Nationwide distribution in the states of AL,AR, AZ, CA, FL, ID, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NV, NY, OH, OK, OR, PA, RI, SC, SD, TX, UT, VA , WA WI and WV. and Foreign countries.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    In affected Artis systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement.