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Class I Recall of Zimmer Biomet ROSA Robotic Surgery System

10:26 EST 7 Nov 2019 | Medscape

The recall stemmed from a software issue with the ROSA 3.0 system that incorrectly positions the robotic arm, potentially leading to serious injury or death, an FDA statement said.
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Original Article: Class I Recall of Zimmer Biomet ROSA Robotic Surgery System

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