Z-0976-03

Magnetom Symphony/Sonata, OR Table

Name: Z-0976-03 Magnetom Symphony/Sonata, OR Table
Creator: Siemens Medical Solutions USA, Inc
Published: 2002-11-27
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2002-11-27 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Magnetom Symphony/Sonata, OR Table on 2002-11-27. The reason FDA records is "OR Table stops during the transfer of the table to the MR system and will not move". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0976-03
Status: Terminated
Initiated: 2002-11-27
Posted: 2003-07-03
Terminated: 2004-05-11
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Magnetom Symphony/Sonata, OR Table.
Product code: LNH System, Nuclear Magnetic Resonance Imaging
Reason for recall: OR Table stops during the transfer of the table to the MR system and will not move.
FDA root cause: Other
Action: Customer Advisory Letter, number 01/2002 titled ''Potential Fault condition of the OR-Table in combination with Magnetom Symphony/Sonata' was sent out to the 2 hospitals in November, 2002.
Quantity in commerce: 2
Distribution: CA, TX .
Product codes and lots: Serial Numbers 021107 and 021941.

Product code LNH

K012495Class IIOr Table and Headholder/magnetom Harmony, Symphony, Sonata SystemsSiemens Medical Solutions USA, Inc. / cleared 2001-10-31

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)