FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: Magnetom Trio magnetic resonance imaging
- Recall number
- Z-0225-2007
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- Magnetom Trio magnetic resonance imaging
- Status
- Terminated
- Initiated
- 2006-10-12
- Posted
- 2006-11-29
- Terminated
- 2008-04-23
- Reason
- Possible excessive RF exposure/may burn
- Root cause
- Other
- Action
- The recalling firm has issued a Customer Safety Advisory to affected customers per Update Instructions MR038/06/S. The letter informs customers of the potential issue and instructs them not to use the involved coils until this issue can be corrected.
- Quantity
- 12 units
- Distribution
- Nationwide.
- Lot, serial or model codes
- Model number 7387074. Serial numbers 20596, 20602, 20613, 20601, 20567, 20557, 20507, 20554, 20559, 20523, 20577, and 20565.
- 510(k) numbers
- ["K050200"]
- PMA numbers
- not on file
- Product code
- LNH
- 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