Z-0769-2007

Magnetom Espree System with OR Table

Name: Z-0769-2007 Magnetom Espree System with OR Table
Creator: Siemens Medical Solutions USA, Inc
Published: 2007-03-30
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2007-03-30 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Magnetom Espree System with OR Table on 2007-03-30. The reason FDA records is "If table top is not seated properly it can lock up/stick". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0769-2007
Status: Terminated
Initiated: 2007-03-30
Posted: 2007-04-26
Terminated: 2007-08-07
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Magnetom Espree System with OR Table
Product code: LNH System, Nuclear Magnetic Resonance Imaging
Reason for recall: If table top is not seated properly it can lock up/stick.
FDA root cause: Other
Action: The recalling firm issued a Safety Advisory Letter to their customers on March 30, 2007, informing them of the problem and steps to take to avoid the problem.
Quantity in commerce: 3 units
Distribution: The product was shipped to medical facilities in NY and TX.
Product codes and lots: Model number 10092082, serial number 1002, 1003, and 1004.

Product code LNH

K041112Class IIMagnetom Espree SystemSiemens Medical Solutions USA, Inc. / cleared 2004-07-21

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)