Siemens Artis zee biplane-Interventional Fluoroscopic recall
Siemens Artis zee biplane-Interventional Fluoroscopic X-Ray System Model Number: 10094141
Why was Siemens Artis zee biplane-Interventional Fluoroscopic recalled?
Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel
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 Numbers: 153883 154041 153640 153772 154007 153870 153762 153700 153797 153827 153898 153779 153869 153952 153736 153829 153763 153998 153819 153758 153928 153760 153865 153903 153908 154592 153863 154785 154079 153988 153882 153831 153939 153875 153847 153930 153913 153890 153922 153992 153916 153975 154012 153947 154076 154086 154058 154028 154073 154048 154034 153987 154093 154090 154074 154052 154075 154406 154408 154459 154425 154423 154502 154084 154579 154546 154085 154471 154453 154097 154098 154544 154663 154576 154572 154560 154584 154571 154096 154514 154556 154509 154731 154536 154564 154739 154596 155147 154783 154653 154732 154687 154685 154779 154708 155150 154709 154715 154789 131011 131224 154800 131013 155119 131101 154814 131105 155122 131108 131110 155126 155131 155148 155189 131223 155195 131219 155203 155235 131231
- Product
- Siemens Artis zee biplane-Interventional Fluoroscopic X-Ray System Model Number: 10094141
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 120
- Distribution
- Nationwide
- Recall date
- July 10, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)