Siemens Axiom Artis U mobile x-ray system Product Usage: Mobile x-ray system
FDA device recall Z-3009-2011 · posted 2011-08-11 · Terminated
Recall details
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Reason for recall
- When the heat unit of the angiography system reaches or exceeds 65%, the cool down time display will appear with an acoustic signal. If users ignore the warning and continue the radiation, the tube may be autoprotected when it reaches its temperature limitation causing the X-Ray to lock until the tube cools down. Following a tube auto-protection, an error message "Door is Open" or "Err 421/240:
- Action taken
- Siemens sent a "Customer Safety Advisory Notice" letters to all affected users dated June 13, 2011. The letter identified the product, the problem, and the actions to be taken. Siemens included in the notice an addendum to the instruction for use to each system and request customers to take special attention. Customers were instructed to place the Safety Notice in the System's instruction for use. All appropriate personnel should be notified of the correction notice. If product was distributed further, customers were to forward the safety notice to the new owner and inform the firm of the new owner.
- Root cause
- Labeling False and Misleading
- Status
- Terminated
- Product code
- IZL
- Quantity affected
- 18
- Distribution
- Nationwide Distribution (USA) including the states of: CA, CT, FL, KS, MN, MO, NJ, NY, NC, PA, and UT.
- Date initiated
- 2011-06-29
- Date posted
- 2011-08-11
- Date terminated
- 2014-01-24
- Location
- Malvern, PA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| AXIOM ARTIS U (K040675) | Siemens Medical Systems, Inc. | 2004-06-10 |