FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: MAGNETOM Verio Nuclear magnetic resonance imaging
- Recall number
- Z-1401-2011
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- MAGNETOM Verio Nuclear magnetic resonance imaging
- Status
- Terminated
- Initiated
- 2011-01-10
- Posted
- 2011-02-23
- Terminated
- 2012-09-25
- Reason
- On some systems the gradient cable connections did not meet firm's specifications after installation
- Root cause
- Other
- Action
- Siemens Medical Solutions USA, Inc sent customers a letter on January 10, 2011 notifying them of an Update Instruction and informing them that recalling firm would preventatively check the gradient cable connections of all systems. For questions regarding this recall call 610-219-6300.
- Quantity
- 92
- Distribution
- Nationwide Distribution including AK, AZ, CA, CT, FL, HI, IL, IN, KY, MA, MD, MI, MN, MO, MT, NC, NJ, NM, NV, OH, OK, OR, PA, RI, TN, TX, VA, WI, and WV
- Lot, serial or model codes
- Model number 10276755
- 510(k) numbers
- ["K072237"]
- PMA numbers
- not on file
- Product code
- LNH
- 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