Z-0009-04

Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive

Name: Z-0009-04 Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive
Creator: Siemens Medical Solutions USA, Inc
Published: 2003-08-08
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2003-08-08 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive on 2003-08-08. The reason FDA records is "possible movement of table tilt and table longitudinal". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0009-04
Status: Terminated
Initiated: 2003-08-08
Posted: 2003-10-15
Terminated: 2004-01-16
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive
Product code: JAA System, X-Ray, Fluoroscopic, Image-Intensified
Reason for recall: possible movement of table tilt and table longitudinal
FDA root cause: Other
Action: The recalling firm issued Update Instructions SP016/03/S, SP017/03S and SP018/03/S that instruct the Service Engineers to visit each affected system to install the required parts.
Quantity in commerce: 34 units
Distribution: Nationwide. The product was shipped to medical facilities in CA, FL, GA, IL, MD, NC, NJ, NY, OK, PA, SC, TN, TX, VA, WI, and WV.
Product codes and lots: Uroskop D1/D2/D3

Product code JAA

K923049Class IIUroskop D1, Uroskop D2, and Uroskop D3Siemens Medical Solutions USA, Inc. / cleared 1992-09-15

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)