MAGNETOM Verio recallZ-1401-2011 · Siemens Medical Solutions USA, Inc · initiated Jan 10, 2011
Terminated All recalls posted in February 2011
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Siemens Medical Solutions USA, Inc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
On some systems the gradient cable connections did not meet firm's specifications after installation
FDA root cause category: Other
What the company is doing
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.
Recall details
- Recall number
- Z-1401-2011
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Jan 10, 2011
- Posted by the FDA
- Feb 23, 2011
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 92
- Product code
- LNH
- FDA submissions
- K072237
- 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
Product description
MAGNETOM Verio Nuclear magnetic resonance imaging
Code information (models, lots, serial numbers)
Model number 10276755
Other devices under the same FDA submission
1 device cleared under K072237 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- MAGNETOM Verio 10684334Siemens Healthcare GmbH · System, nuclear magnetic resonance imaging3 recalls1 report
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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