Z-0226-2007

Magnetom Trio TIM, magnetic resonance imaging

Name: Z-0226-2007 Magnetom Trio TIM, magnetic resonance imaging
Creator: Siemens Medical Solutions USA, Inc
Published: 2006-10-12
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2006-10-12 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Magnetom Trio TIM, magnetic resonance imaging on 2006-10-12. The reason FDA records is "Possible excessive RF exposure/may burn". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0226-2007
Status: Terminated
Initiated: 2006-10-12
Posted: 2006-11-29
Terminated: 2008-04-23
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Magnetom Trio TIM, magnetic resonance imaging
Product code: LNH System, Nuclear Magnetic Resonance Imaging
Reason for recall: Possible excessive RF exposure/may burn
FDA 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 in commerce: 9 units
Distribution: Nationwide.
Product codes and lots: Model number 10018221. Serial numbers 35114, 35115, and 35177. Model number 10018222. Serial numbers 35025, 35006, 35022, 35008, 35014, and 35019.

Product code LNH

K050200Class IIMagnetom Trio a Tim SystemSiemens Medical Solutions USA, Inc. / cleared 2005-02-28

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)