FDA Medical devices recall ·
MAGNETOM Verio Dot Upgrade recall
This is an FDA Class I recall — the most serious type.
- Recall number
- Z-2666-2025
- Date
- (initiated August 28, 2025)
- Company / brand
- Siemens Medical Solutions USA, Inc
40 Liberty Blvd, Malvern, PA, United States - Category
- Medical devices › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 78 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
MAGNETOM Verio Dot Upgrade. Model Number: 10684334.
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Model Number: 10684334. UDI Numbers: (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, (
Distribution
Worldwide distribution - US Nationwide and the countries of United Arab Emirates, Armenia, Angola, Argentina, Austria, Australia, Azerbaijan, Bosnia and Herzegovina, Bangladesh, Belgium, Bulgaria, Bahrain, Brunei Darussalam, Brazil, Botswana, Belarus, Canada, Switzerland, Chile, China, Colombia, Cyprus, Czechia, Germany, Denmark, Algeria, Ecuador, Estonia, Egypt, Spain, Ethiopia, Finland, Faroe Islands, France, United Kingdom of Great Britian and Northern Ireland, Georgia, Greece, Hong Kong, Croatia, Hungary, Canary Islands, Indonesia, Ireland, Israel, India, Iran, Iceland, Italy, Jordan, Japan, Kenya, Korea, Kuwait, Kazakhstan, Lebanon, Sri Lanka, Lithuania, Luxembourg, Latvia, Morocco, Monaco, Moldova, Montenegro, Republic of North Macedonia, Myanmar, Mongolia, Macao, Malta, Maldives, Mexico, Malaysia, Mozambique, Nigeria, Netherlands, Norway, Nepal, New Zealand, Oman, Panama, Peru, Philippines, Pakistan, Poland, Portugal, Paraguay, Qatar, Reunion, Romania, Serbia, Russian Federation, Saudi Arabia, Sweden, Singapore, Slovenia, Slovakia, Senegal, Syrian Arab Republic, Thailand, Turkmenistan, Tunisia, Turkey, Trinidad and Tobago, Taiwan, Tanzania, Ukraine, Uganda, Uzbekistan, Viet Nam, Kosovo, South Africa.
States: Georgia
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (medical devices), recall Z-2666-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.