ClearanceBrief
Recall Z-0639-2018 ยท OLO Orthopedic Stereotaxic Instrument

Zimmer Biomet, Inc.

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.

DateMay 1, 2017
StatusTerminated
ReasonRobot arm being sent to the wrong position
Root causeSoftware design
ActionUrgent Medical Device Recall (Correction) notices were sent to customers. The letter provided to hospital risk managers and surgeons identified the issue and their responsibilities. These responsibilities included: - Stop using the micromovement function in isocentric mode during Brain Surgery with ROSA Brain 3.0 device. -Reviewing the notification to ensure comprehension of the steps required to be taken prior to the permanent correction that will be implemented on site by a service engineer. - Completing and returning Attachment 1 (Certificate of Acknowledgement) to the e-mail address provi
Quantity1
DistributionDistributed to CA, DC, FL, IL, KY, MA, MN, NC, NY, OH, and PA.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K151511ROSA Spine
Medtech S.A, Jan 4, 2016