FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: Mobilett XP Hybrid/Digital/CR Intended use: mobile x-ray system
- Recall number
- Z-0718-2011
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- Mobilett XP Hybrid/Digital/CR Intended use: mobile x-ray system
- Status
- Terminated
- Initiated
- 2010-10-04
- Posted
- 2010-12-17
- Terminated
- 2012-09-29
- Reason
- battery fuse
- 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: meredith.adams@siemens.com and Director, Product complaints & Field Support by phone 610-448-4634 or email: josephine.mcbride@siemens.com.
- Quantity
- 170 units
- Distribution
- Nationwide distribution: AZ, CA, DC, MD, PA, SC and VA.
- Lot, serial or model codes
- Model numbers 1818454, 1818447, and 1818959
- 510(k) numbers
- ["K033238"]
- 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