{"id":"cdc6c5a0-d046-4fd3-a7b2-e065009851fe","slug":"zimmer-rosa-brain-3-arm-wrong-position-recall-2018","kind":"recall","headline":"Zimmer Biomet recalls ROSA Brain 3.0 over the robotic arm being sent to the wrong position","summary":"Zimmer Biomet recalled the ROSA Brain 3.0 stereotactic neurosurgery robot because the robotic arm could be sent to the wrong position. 16 units. 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Source: FDA Class 2 device recall Z-0638-2018, openFDA enforcement / accessdata.fda.gov.","identifier":"cdc6c5a0-d046-4fd3-a7b2-e065009851fe","datePublished":"2017-05-01T00:00:00.000Z","articleSection":"recall","publisher":{"@id":"https://deploy.report/#organization"},"author":{"@id":"https://deploy.report/#organization"}},"framework_metadata":{"framework_schema_version":"0.1.0","verification_status":"verified","maturity_stage":null,"lifecycle_state":null,"architectural_position":{"cohort":null,"sub_cohorts":[]},"within_cohort_verified_vs_claimed_pair":null,"cap_flags":[],"verification_depth":{"sources_count":1,"primary_source_types":["primary-fda-database"]}}}