Z-1476-04

Siregraph CF X-Ray System. Fluoroscopic image intensified. Model number 4466041

Name: Z-1476-04 Siregraph CF X-Ray System. Fluoroscopic image intensified. Model number 4466041
Creator: Siemens Medical Solutions USA, Inc
Published: 2004-06-07
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2004-06-07 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Siregraph CF X-Ray System. Fluoroscopic image intensified. Model number 4466041 on 2004-06-07. The reason FDA records is "X-ray tube movement when table is tilted more than 90 degrees". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1476-04
Status: Terminated
Initiated: 2004-06-07
Posted: 2004-09-18
Terminated: 2005-08-18
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Siregraph CF X-Ray System. Fluoroscopic image intensified. Model number 4466041
Product code: JAA System, X-Ray, Fluoroscopic, Image-Intensified
Reason for recall: X-ray tube movement when table is tilted more than 90 degrees
FDA root cause: Other
Action: The recalling firm issued a Customer DAfety Advisory letter dated 6/7/04 to the hospitals. The letter informs them of the potential problem and provides preventative measures to avoid its occurance.
Quantity in commerce: 1 unit
Distribution: The products were shipped to medical facilities in FL, IL, MI, NH, NJ, PA, and TX.
Product codes and lots: Serial number: 3131.

Product code JAA

K960266Class IISiregraph CfSiemens Medical Solutions USA, Inc. / cleared 1996-03-11

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)