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Recall Observatory FDA recall evidence

Device product

ROSA Surgical Device 2.5.8 It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial markers or optical registration. The system is intended for use by neurosurgeons to guide standard neurosurgical instruments. It is indicated for any neurosurgical condition in which the use of stereotactic surgery may be appropriate.

Z-0161-2018

June 04, 2014

Class II

Product summary

Firm
Zimmer Biomet, Inc.
Event
Event 77750
Status
Terminated
Classification
Class II
Quantity
29 devices(8 US and 21 OUS)
Official record key
device-enforcement:Z-0161-2018

Official wording

Reason: Software corrections reactivating the cooperative endoscopy mode.

Code information: Serial No. RO10011, RO14033, RO14031, RO14035, RO13027, RO13023, RO10014, RO10009, RO10010, RO14030, RO11016, RO11017, RO12022, RO14029, RO14032, RO08003, RO09004, RO10007, RO10013, RO12018, RO12019, RO13025, RO14034, RO11015, RO13024, RO09005, RO13026, RO12021, and RO12020.

Distribution pattern: Worldwide distribution: US (nationwide) in states of: AR, GA, MI, OH, and TX; and countries of:Canada, China, France, Germany, Israel, Italy, Russia, Saudi Arabia, and Spain.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Software corrections reactivating the cooperative endoscopy mode.