Z-1528-05

Magnetom Avanto. Magnetic Resonance Imaging System. Model number 7391167

Name: Z-1528-05 Magnetom Avanto. Magnetic Resonance Imaging System. Model number 7391167
Creator: Siemens Medical Solutions USA, Inc
Published: 2005-08-12
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2005-08-12 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Magnetom Avanto. Magnetic Resonance Imaging System. Model number 7391167 on 2005-08-12. The reason FDA records is "there is a misalignment of the patient table that may occur between the patient table and the opening to the magnet bore". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1528-05
Status: Terminated
Initiated: 2005-08-12
Posted: 2005-09-09
Terminated: 2006-07-19
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Magnetom Avanto. Magnetic Resonance Imaging System. Model number 7391167
Product code: LNN
Reason for recall: there is a misalignment of the patient table that may occur between the patient table and the opening to the magnet bore
FDA root cause: Other
Action: The recalling firm issued via certified mail a Customer Safety Advisory to the affected customers per Update Instructions MR031/05/S. the letter informs customers of the potential issue and provides instructions to avoid its occurrence.
Quantity in commerce: 209 units
Distribution: The products were shipped to medical facilities and MRI facilities nationwide.
Product codes and lots: Serial numbers 25007 to 25557

Product code LNN

K032428Class IIMagnetom Avanto Mr SystemSiemens Medical Solutions USA, Inc. / cleared 2003-10-16

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)