Reported Oct 8, 2025 · Ongoing
MAGNETOM Verio Dot Upgrade. Model Number: 10684334.
Siemens Medical Solutions USA, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Siemens Medical Solutions USA, Inc · 40 Liberty Blvd · Malvern, PA · 19355-1418
Is this the product you have?
- MAGNETOM Verio Dot Upgrade
- Model Number10684334
- Lot codes and dates
- Model Number10684334
- UDI Numbers
78 of 78 codes
(01)04056869006680(21)162012(01)04056869006680(21)162055(01)04056869006680(21)162039(01)04056869006680(21)162002(01)04056869006680(21)162014(01)04056869006680(21)162069(01)04056869006680(21)162083(01)04056869006680(21)162075(01)04056869006680(21)162028(01)04056869006680(21)162060(01)04056869006680(21)162035(01)04056869006680(21)162038(01)04056869006680(21)162016(01)04056869006680(21)62040(01)04056869006680(21)162036(01)04056869006680(21)162079(01)04056869006680(21)162054(01)04056869006680(21)162088(01)04056869006680(21)162071(01)04056869006680(21)162078(01)04056869006680(21)62032(01)04056869006680(21)62037(01)04056869006680(21)162077(01)04056869006680(21)162042(01)04056869006680(21)162025(01)04056869006680(21)162082(01)04056869006680(21)162085(01)04056869006680(21)162026(01)04056869006680(21)62027(01)04056869006680(21)162040(01)04056869006680(21)162032(01)04056869006680(21)162072(01)04056869006680(21)162037(01)04056869006680(21)162043(01)04056869006680(21)62014(01)04056869006680(21)162047(01)04056869006680(21)162023(01)04056869006680(21)62019(01)04056869006680(21)62050(01)04056869006680(21)162089(01)04056869006680(21)162061(01)04056869006680(21)62018(01)04056869006680(21)162004(01)04056869006680(21)162080(01)04056869006680(21)162013(01)04056869006680(21)162007(01)04056869006680(21)162049(01)04056869006680(21)162031(01)04056869006680(21)162009(01)04056869006680(21)162008(01)04056869006680(21)62029(01)04056869006680(21)162056(01)04056869006680(21)62025(01)04056869006680(21)62022(01)04056869006680(21)162048(01)04056869006680(21)62036(01)04056869006680(21)162087(01)04056869006680(21)162081(01)04056869006680(21)162073(01)04056869006680(21)162044
- Serial Numbers
78 of 78 codes
162012162055162039162002162014162069162083162075162028162060162035162038162016620401620361620791620541620881620711620786203262037162077162042162025162082162085162026620271620401620321620721620371620436201416204716202362019620501620891620616201816200416208016201316200716204916203116200916200862029162056620256202216204862036162087162081162073162044
- Amount recalled
- 78 units
This recall covers 15 products
The agency filed one notice per product. You are reading one of them; the other 14 are below.
2 more are in the archive.
Where it was sold
- Nationwide
- GA
Why it was recalled
Stop using this product now
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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