Zimmer Biomet Issues Voluntary Field Action on Rosa Platforms

Zimmer Biomet issued a voluntary field safety corrective action for certain ROSA Brain, ROSA Spine and ROSA One devices due to internal identification of an issue that may prevent the robot arm from reaching a desired position. The issue has not been identified in the field.

Affected units were distributed between June 2015 and April 2017.

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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