FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: Mobilett XP and Mobilett XP Hybrid, Mobile radiology device System, x-ray, mobile
- Recall number
- Z-0171-2011
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- Mobilett XP and Mobilett XP Hybrid, Mobile radiology device System, x-ray, mobile
- Status
- Terminated
- Initiated
- 2010-10-04
- Posted
- 2010-11-01
- Terminated
- 2012-09-29
- Reason
- Units not equipped with protective plastic cover over electronics.
- Root cause
- Device Design
- Action
- Siemens Medical Solutions USA, Inc issued a mandatory field update. The letter identified the product, the problem and the action to be taken by the customer. All systems that were not yet equipped with protective cover over the D972 board would be upgraded. For questions regarding this recall call (610) 448-3237.
- Quantity
- 177 units
- Distribution
- Nationwide Distribution including AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, LA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, PA, TX, VA, WA, WI, WY AND PUERTO RICO.
- Lot, serial or model codes
- Model numbers 1818363 and 1818454
- 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