Z-0168-2007

Modularis URO urological table Model number 5531012

Name: Z-0168-2007 Modularis URO urological table Model number 5531012
Creator: Siemens Medical Solutions USA, Inc
Published: 2006-10-01
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2006-10-01 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Modularis URO urological table Model number 5531012 on 2006-10-01. The reason FDA records is "Potential pinch point with the patient table". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0168-2007
Status: Terminated
Initiated: 2006-10-01
Posted: 2006-11-14
Terminated: 2008-05-13
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Modularis URO urological table Model number 5531012
Product code: MMZ Table, Cystometric, Electric
Reason for recall: Potential pinch point with the patient table
FDA root cause: Other
Action: The recalling firm has issued a Customer Safety Advisory to affected customers per Update Instructions SPO23/06/S. This letter, to be inserted in the system Operator Manual, reminds customers of the potential pinch point and provides a suggestion to avoid its occurrence.
Quantity in commerce: 59 units
Distribution: Nationwide.
Product codes and lots: Model number 5531012, serial numbers 01001 to 01345

Product code MMZ

K033335Class IILithostar Modularis with Shockwave System CplusSiemens Medical Solutions USA, Inc. / cleared 2003-11-25

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)