{"id":"7d721484-e29c-4319-b46a-0ab954cee00e","slug":"hocoma-lokomat-fda-recall-2009","kind":"recall","headline":"FDA Class 2 recall of Hocoma Lokomat System due to software sensitivity bug","summary":"Hocoma issued a field safety notice for the Lokomat System with Pediatric Module (software versions V4.30 through V5.0x) after discovering that changes to stored sensitivity values could lead to higher limits in force and trajectory deviation. 7 units were distributed across IL, MA, MI, NY, and OH. The FDA classified this as a Class 2 recall. 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Founded in 1996 in Volketswil near Zurich by Dr. Gery Colombo, Matthias Jörg, and Peter Hostettler, the company merged with Hong Kong-based [DIH International](https://www.dih.com) in 2016 and became a wholly-owned subsidiary of DIH Nevada as of July 2021. 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