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FDA (Device enforcement)Recalled 2025-08-28class i

Siemens Medical Solutions USA, Inc: BIOGRAPH One (DE). Model Number: 11689172.

Hazard

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.

Details from the source

Reason for recall: 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. 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 Is Quantity: 1 unit Lot/code info: Model Number: 11689172. UDI Numbers: (01)4068151020472(21)238008. Serial Number: 238008.

UPC codes

4068151020472

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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