Artis Q recall
Artis Q (material 10848280, 10848281, 10848282) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography systems developed…
Why was Artis Q recalled?
In affected Artis systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial Number 103302 103279 103285 103286 103277 103295 103310 103293 109569 109502 109592 109523 109583 109512 109496 109542 109589 109552 109598 109500 109504 109505 109526 109565 109536 109520 109501 109507 109567 109541 109515 109551 109518 109538 109531 109532 109543 109503 109497 109527 109560 109564 109558 109524 109525 109591 121471 121467 121501 121445 121459 121490 121461 121491 121455 121504 121457 121460 121493 121487 121472 121478 121479 121470 121485 121486 121462 121468 121505 121506 121502
- Product
- Artis Q (material 10848280, 10848281, 10848282) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography systems developed…
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 459 (116 US)
- Distribution
- 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.
- Recall date
- May 22, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)