Z-0718-2011

Mobilett XP Hybrid/Digital/CR

Name: Z-0718-2011 Mobilett XP Hybrid/Digital/CR
Creator: Siemens Medical Solutions USA, Inc
Published: 2010-10-04
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2010-10-04 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Mobilett XP Hybrid/Digital/CR Intended use: mobile x-ray system on 2010-10-04. The reason FDA records is "battery fuse". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0718-2011
Status: Terminated
Initiated: 2010-10-04
Posted: 2010-12-17
Terminated: 2012-09-29
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Mobilett XP Hybrid/Digital/CR Intended use: mobile x-ray system
Product code: IZL System, X-Ray, Mobile
Reason for recall: battery fuse
FDA root cause: Other
Action: SIEMENS released a field update dated October 25, 2010, via SP011/10/S to the representatives. The update described issue and corrective action plan. The representatives are to visit each account to upgrade the systems with a new battery fuse and a new holder. If you have any questions regarding this report, please contact Quality Engineer by phone 610-448-3237 or email: [email protected] and Director, Product complaints & Field Support by phone 610-448-4634 or email: [email protected].
Quantity in commerce: 170 units
Distribution: Nationwide distribution: AZ, CA, DC, MD, PA, SC and VA.
Product codes and lots: Model numbers 1818454, 1818447, and 1818959

Product code IZL

K033238Class IIMobilette Xp and Mobilett XphybridSiemens Medical Systems, Inc. / cleared 2003-11-14

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 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)