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Zimmer Biomet, Inc. recalls ROSA Surgical Device 2.5.8
Recalled December 6, 2017 · FDA recall Z-0178-2018 · Zimmer Biomet
Hazard
Issue with optional neuro-endoscopy module detected under specific conditions during internal testing. · FDA Class II
Units
22 units (4 US and 18 OUS)
Sold at
AR, OH, MI, and TX
Description
Issue with optional neuro-endoscopy module detected under specific conditions during internal testing.
Product
ROSA Surgical Device 2.5.8
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →