FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
- Recall number
- Z-1080-2014
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
- Status
- Terminated
- Initiated
- 2013-12-16
- Posted
- 2014-02-24
- Terminated
- 2015-03-09
- Reason
- During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage.
- Root cause
- Device Design
- Action
- In December 2013, a recall notification letter was sent to Users.
- Quantity
- 284
- Distribution
- Nationwide Distribution.
- Lot, serial or model codes
- Artis zee Ceiling systems serial numbers from 146352 to 147617
- 510(k) numbers
- ["K073290"]
- 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