FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: AXIOM Artis MP, Angiographic x-ray system, model number 7555365
- Recall number
- Z-0579-2007
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- AXIOM Artis MP, Angiographic x-ray system, model number 7555365
- Status
- Terminated
- Initiated
- 2007-01-31
- Posted
- 2007-03-08
- Terminated
- 2009-05-05
- Reason
- C-arm gantry could rapidly descend without command during use
- Root cause
- Other
- Action
- In response to this issue, a Siemens Service Representative will visit the affected consignees beginning 02/01/2007, to check the spindle and adjust the spindle, if necessary.
- Quantity
- 8 units
- Distribution
- The products were shipped to medical facilities nationwide.
- Lot, serial or model codes
- Model number 7555365 - serial numbers 57004, 57008, 57009, 57012, 57045, 57016, 57024 and 57041
- 510(k) numbers
- ["K010721"]
- PMA numbers
- not on file
- Product code
- IZI
- Firm FEI
- 2240869
- Firm city
- Malvern
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28