Z-0522-04

Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device

Name: Z-0522-04 Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device
Creator: Siemens Medical Solutions USA, Inc
Published: 2003-12-18
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2003-12-18 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device on 2003-12-18. The reason FDA records is "tissue roll can become magnetic". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0522-04
Status: Terminated
Initiated: 2003-12-18
Posted: 2004-02-10
Terminated: 2004-11-09
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device
Reason for recall: tissue roll can become magnetic
FDA root cause: Other
Action: The recalling firm has issued Updated Instructions to replace the stainless steel tissue roll holder. The recalling firm''s representatives are visiting each account to replace the tissue roll holder.
Quantity in commerce: 16 units
Distribution: The product was shipped to medical facilities in CA, CT, DC, FL, GA, IL, IN, KS, KY, MA, MD, MN, NC, NY, OH, OR, PA, TX, and UT.
Product codes and lots: Model #7106433 - Serial #''s 20101 through 20113. Model #7387736 - Serial #''s 20405, 20406, 20411, 20412, and 20419

K002179Class IIMagnetom Allegra SystemSiemens Medical Solutions USA, Inc. / cleared 2000-10-11

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)