Z-0750-2007

Mobilett XP, mobile X-ray system, Model number 1818447

Name: Z-0750-2007 Mobilett XP, mobile X-ray system, Model number 1818447
Creator: Siemens Medical Solutions USA, Inc
Published: 2007-03-21
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2007-03-21 / Terminated

FDA source

Siemens Medical Solutions USA, Inc began a recall of Mobilett XP, mobile X-ray system, Model number 1818447 on 2007-03-21. The reason FDA records is "Mounting bolts for tank fork assembly and collimator flange may become loose". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0750-2007
Status: Terminated
Initiated: 2007-03-21
Posted: 2007-04-19
Terminated: 2007-08-07
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Mobilett XP, mobile X-ray system, Model number 1818447
Product code: IZL System, X-Ray, Mobile
Reason for recall: Mounting bolts for tank fork assembly and collimator flange may become loose.
FDA root cause: Other
Action: Siemens Service Personnel are visiting each consignee, beginning March 21, 2007, to replace the required mounting bolts and tighten them according to required torque specifications.
Quantity in commerce: 36 units
Distribution: The products were shipped to medical facilities nationwide.
Product codes and lots: Serial numbers 2033, 1034, 1010, 1020, 1041, 1053, 2044, 2045, 1008, 1043, 1025, 1026, 1027, 1028, 1029, 1030, 1031, 1032, 1033, 1040, 2007, 1052, 2001, 1017, 2002, 2040, 2021, 2022, 1011, 1016, 1018, 1021, 1039, 1054, 2005, and 2017.

Product code IZL

The FDA recall record names no cleared device, and no clearance has been matched to it.

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)