FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: 3D Ceiling Suspension
- Recall number
- Z-0987-03
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- 3D Ceiling Suspension
- Status
- Terminated
- Initiated
- 2003-04-15
- Posted
- 2003-07-10
- Terminated
- 2005-04-11
- Reason
- the back up safety catch may not function properly
- Root cause
- Other
- Action
- Letters dated 4/15/03 and 4/23/03 were issued to the accounts along with instructions on how to fix the problem.
- Quantity
- 3504 units
- Distribution
- The product was shipped nationwide to medical facilities.
- Lot, serial or model codes
- all serial numbers
- 510(k) numbers
- ["K790765","K803130"]
- PMA numbers
- not on file
- Product code
- IZF
- 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