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Siemens Medical Solutions USA, Inc. recalls ACUSON Juniper Diagnostic Ultrasound System
Recalled September 22, 2021 · FDA recall Z-2471-2021 · Siemens Medical Solutions USA
Hazard
Due to intermittent failures of the power supply in the ultrasound system which renders it inoperable. · FDA Class II
Units
15 systems
Sold at
Worldwide distribution - U.S. Nationwide distribution in the Puerto Rico and the countries of Bosnia Herzegovina, Canada, Colombia, Germany, Greece, Italy, North Macedonia, Poland, and Slovenia.
Description
Due to intermittent failures of the power supply in the ultrasound system which renders it inoperable.
Product
ACUSON Juniper Diagnostic Ultrasound System
Manufacturer(s)
Siemens Medical Solutions USA, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →