Z-0890-2007

Sienet MagicStore. Radiological Digital Image Communications System

Name: Z-0890-2007 Sienet MagicStore. Radiological Digital Image Communications System
Creator: Siemens Medical Solutions USA, Inc
Published: 2007-05-02
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2007-05-02 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Sienet MagicStore. Radiological Digital Image Communications System on 2007-05-02. The reason FDA records is "System could crash and result in data loss". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0890-2007
Status: Terminated
Initiated: 2007-05-02
Posted: 2007-06-05
Terminated: 2008-09-17
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Sienet MagicStore. Radiological Digital Image Communications System
Product code: LMD System, Digital Image Communications, Radiological
Reason for recall: System could crash and result in data loss.
FDA root cause: Other
Action: The recalling firm issued a Safety Advisory letter to their customers (May 2, 2007) to inform them of the problem. A company representative will be contacting the customers to arrange for replacement of the RAID component.
Quantity in commerce: 19 units
Distribution: The products were shipped to medical facilities in CA, CO, FL, MS, NH, NJ, NY, and WA.
Product codes and lots: Model number 7502052 Serial numbers 1793, 1804, 1867, 1920, 1966, 1968, 1983, 2055, 2099, 2527, 2601, 2610, 2618, 2632, 2635, 2638, 2678, 2686, and 2689.

Product code LMD

K920310Class ISienet Archive Server, Isa I, Isa II Storage ServeSiemens Gammasonics, Inc. / cleared 1992-03-30

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)