Siemens Artis Q floor --Interventional Fluoroscopic recall
Siemens Artis Q floor --Interventional Fluoroscopic X-Ray System Model Number: 10848280
Why was Siemens Artis Q floor --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: 103008 103030 103028 103258 103221 103222 103277 103220 103279 103285 103286 103295
- Product
- Siemens Artis Q floor --Interventional Fluoroscopic X-Ray System Model Number: 10848280
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 12
- Distribution
- Nationwide
- Recall date
- July 10, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)