Zimmer Biomet, Inc. recalls ROSA Surgical Device 2.5.8
- Recall date
- February 10, 2013
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0178-2018
- FDA classification
- Class II
- Brand / firm
- Zimmer Biomet, Inc.
- Sold / distributed
- AR, OH, MI, and TX
Why it was recalled
Issue with optional neuro-endoscopy module detected under specific conditions during internal testing.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
ROSA Surgical Device 2.5.8
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