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U.S. Department of Health and Human Services

Class 2 Device Recall Computer Assisted Surgical Device

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  Class 2 Device Recall Computer Assisted Surgical Device see related information
Date Initiated by Firm April 19, 2012
Create Date November 16, 2017
Recall Status1 Terminated 3 on June 16, 2020
Recall Number Z-0100-2018
Recall Event ID 77667
510(K)Number K101791  K092239  
Product Classification Neurological stereotaxic Instrument - Product Code HAW
Product ROSA Surgical Device 2.5.8
ROSA Surgical Device is a computer-controlled electromechanical arm. 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
Code Information Serial No. RO10011 and RO10014
Recalling Firm/
Manufacturer		 Zimmer Biomet, Inc.
1800 W Center St
Warsaw IN 46580-2304
For Additional Information Contact Kevin W Escapule
574-267-6131
Manufacturer Reason
for Recall		 Potential failure of the optical distance sensor due to cable disconnection.
FDA Determined
Cause 2		 Device Design
Action Zimmer Biomet sent an Urgent Medical Device Recall Correction letter dated July 26, 2017, to all affected customers. Customers were informed on site of the device correction by Field Service Technicians. For questions regarding this recall call 574-267-6131.
Quantity in Commerce 14 units
Distribution Worldwide Distribution - US including OH and MI Internationally to Canada, China, France, Germany, and Italy
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = HAW and Original Applicant = MEDTECH S.A.
510(K)s with Product Code = HAW and Original Applicant = MEDTECH SAS
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