Zimmer Biomet, Inc. recalls ROSA Spine 1.0.2 Stereotaxic instrument Computer-assisted surgical device. Intended for the spatial positioning and ori…
- Recall date
- May 1, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0639-2018
- FDA classification
- Class II
- Brand / firm
- Zimmer Biomet, Inc.
- Sold / distributed
- Distributed to CA, DC, FL, IL, KY, MA, MN, NC, NY, OH, and PA.
Why it was recalled
Robot arm being sent to the wrong position
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 Spine 1.0.2 Stereotaxic instrument Computer-assisted surgical device. Intended for the spatial positioning and orientation of instrument holders to be used by surgeons.
Get recall alerts
Free email alert whenever Zimmer Biomet, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Zimmer Biomet, Inc.