Siemens Artis Q.zen floor----Interventional recall
Siemens Artis Q.zen floor----Interventional Fluoroscopic X-Ray System Model Number: 10848353
Why was Siemens Artis Q.zen floor----Interventional 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: 105018 105016 105032 105124 105119 105123 105121 105122
- Product
- Siemens Artis Q.zen floor----Interventional Fluoroscopic X-Ray System Model Number: 10848353
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 8
- Distribution
- Nationwide
- Recall date
- July 10, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)