Date Initiated by Firm | February 10, 2013 |
Create Date | November 28, 2017 |
Recall Status1 |
Terminated 3 on June 09, 2020 |
Recall Number | Z-0178-2018 |
Recall Event ID |
77672 |
510(K)Number | K092239 K101791 |
Product Classification |
Neurological stereotaxic Instrument - Product Code HAW
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Product | ROSA Surgical Device 2.5.8 |
Code Information |
Serial No. RO10011, RO10014, RO13023 and RO13027 |
Recalling Firm/ Manufacturer |
Zimmer Biomet, Inc. 1800 W Center St Warsaw IN 46580-2304
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For Additional Information Contact | Kevin Escapule 574-267-6131 |
Manufacturer Reason for Recall | Issue with optional neuro-endoscopy module detected under specific conditions during internal testing. |
FDA Determined Cause 2 | Software design |
Action | Field Service Technicians were dispatched to correct units by upgrading the system to ROSA 2.5.7. A further update of ROSA 2.5.8.4. A Field Safety Notice dated 07/10/2013 notifying consignees of a risk in the ROSA system recognized in internal testing. It was suggested that consignees not utilize the neuro-endoscopy module until further notice. The recall notice should have been shared with the appropriate parties and the signed acknowledgement form returned to the recalling firm. |
Quantity in Commerce | 22 units (4 US and 18 OUS) |
Distribution | AR, OH, MI, and TX |
Total Product Life Cycle | TPLC Device Report |
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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.
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510(K) Database | 510(K)s with Product Code = HAW 510(K)s with Product Code = HAW
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