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Zimmer Biomet, Inc. recalls ROSA Spine 1.0.2 Stereotaxic instrument Computer-assisted surgical device. Intended for the spatial positioning and o
Recalled February 28, 2018 · FDA recall Z-0639-2018 · Zimmer Biomet
Hazard
Robot arm being sent to the wrong position · FDA Class II
Units
1
Sold at
Distributed to CA, DC, FL, IL, KY, MA, MN, NC, NY, OH, and PA.
Description
Robot arm being sent to the wrong position
Product
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.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →