MAGNETOM Verio Nuclear magnetic resonance imaging
FDA device recall Z-1401-2011 · posted 2011-02-23 · Terminated
Recall details
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Reason for recall
- On some systems the gradient cable connections did not meet firm's specifications after installation
- Action taken
- 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.
- Root cause
- Other
- Status
- Terminated
- Product code
- LNH
- Quantity affected
- 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
- Date initiated
- 2011-01-10
- Date posted
- 2011-02-23
- Date terminated
- 2012-09-25
- Location
- Malvern, PA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MAGNETOM VERIO (K072237) | Siemens Medical Solutions USA, Inc. | 2007-10-10 |