Z-1401-2011

MAGNETOM Verio Nuclear magnetic resonance imaging

Name: Z-1401-2011 MAGNETOM Verio Nuclear magnetic resonance imaging
Creator: Siemens Medical Solutions USA, Inc
Published: 2011-01-10
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2011-01-10 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of MAGNETOM Verio Nuclear magnetic resonance imaging on 2011-01-10. The reason FDA records is "On some systems the gradient cable connections did not meet firm's specifications after installation". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1401-2011
Status: Terminated
Initiated: 2011-01-10
Posted: 2011-02-23
Terminated: 2012-09-25
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: MAGNETOM Verio Nuclear magnetic resonance imaging
Product code: LNH System, Nuclear Magnetic Resonance Imaging
Reason for recall: On some systems the gradient cable connections did not meet firm's specifications after installation
FDA root cause: Other
Action: Siemens Medical Solutions USA, Inc sent customers a letter on January 10, 2011 notifying them of an Update Instruction and informing them that recalling firm would preventatively check the gradient cable connections of all systems. For questions regarding this recall call 610-219-6300.
Quantity in commerce: 92
Distribution: Nationwide Distribution including AK, AZ, CA, CT, FL, HI, IL, IN, KY, MA, MD, MI, MN, MO, MT, NC, NJ, NM, NV, OH, OK, OR, PA, RI, TN, TX, VA, WI, and WV
Product codes and lots: Model number 10276755

Product code LNH

K072237Class IIMagnetom VerioSiemens Medical Solutions USA, Inc. / cleared 2007-10-10

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 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)