FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: ONCOR" Expression ONCOR" Impression ONCOR" Impression plus
- Recall number
- Z-1491-2017
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- ONCOR" Expression ONCOR" Impression ONCOR" Impression plus
- Status
- Terminated
- Initiated
- 2017-02-14
- Posted
- not on file
- Terminated
- 2017-12-18
- Reason
- Software update
- Root cause
- Software design
- Action
- Siemens mailed an Customer Information Letter on 02/15/2017 to affected customers to inform them of a software update they plan to implement to reduce risk of collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment table, using the SIMTEC-Auto Field Sequence Option.
- Quantity
- 80 systems
- Distribution
- Distributed throughout the United States
- Lot, serial or model codes
- Device Model# 7360717, 5857920, 5857912
- 510(k) numbers
- ["K060226"]
- PMA numbers
- not on file
- Product code
- IYE
- 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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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