FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: Mobilett XP, mobile X-ray system, Model number 1818447
- Recall number
- Z-0750-2007
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- Mobilett XP, mobile X-ray system, Model number 1818447
- Status
- Terminated
- Initiated
- 2007-03-21
- Posted
- 2007-04-19
- Terminated
- 2007-08-07
- Reason
- Mounting bolts for tank fork assembly and collimator flange may become loose.
- 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
- 36 units
- Distribution
- The products were shipped to medical facilities nationwide.
- Lot, serial or model codes
- 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.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- IZL
- Firm FEI
- 2240869
- Firm city
- Malvern
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28