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Recall Observatory FDA recall evidence

Device product

ROSA Brain 3.0.0 Usage: The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments (biopsy needle, stimulation or recording electrode, endoscope). The device is indicated for any neurosurgical procedure in which the use of stereotactic surgery may be appropriate.

Z-0167-2018

July 20, 2016

Class II

Product summary

Firm
Zimmer Biomet, Inc.
Event
Event 78367
Status
Terminated
Classification
Class II
Quantity
18 (14 US and 4 OUS)
Official record key
device-enforcement:Z-0167-2018

Official wording

Reason: Communication errors between ROSANNA BRAIN software, MARIO software and the St¿ubli CS8C controller.

Code information: Serial #'s: BR16004, BR16005, BR16006, BR16009, BR16010, BR16011, BR16012, BR16013, BR16014, BR16015, BR16016, BR16017, BR16018, and BR16021

Distribution pattern: Worldwide Distribution - US Nationwide in the states of OH, FL, MA, MN, DC, NC, CA, NY, PA and countries of Australia and France

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Communication errors between ROSANNA BRAIN software, MARIO software and the St¿ubli CS8C controller.