Date Initiated by Firm | November 21, 2013 |
Date Posted | February 10, 2014 |
Recall Status1 |
Terminated 3 on July 20, 2015 |
Recall Number | Z-0966-2014 |
Recall Event ID |
66995 |
510(K)Number | K083603 |
Product Classification |
Nystagmograph - Product Code GWN
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Product | Normative Data Template CD for use with the I-Portal devices.
Used to measure, record, or visually display the involuntary movements (nystagmus) of the eyeball. |
Code Information |
Software versions affected: 6.7.004, 6.8. 6.9, 6.10, 7.0, 7.0.1, and 7.1 |
Recalling Firm/ Manufacturer |
Neuro Kinetics, Inc. 128 Gamma Dr Pittsburgh PA 15238-2920
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For Additional Information Contact | Customer Support 412-963-6649 |
Manufacturer Reason for Recall | The data provided on the Normative Data Template CD for use with the I-Portal devices has not received clearance by FDA through the premarket 510(k) notification process. |
FDA Determined Cause 2 | No Marketing Application |
Action | A recall notification letter, dated November 2013, was sent to Users. A follow up letter regarding scheduling removal of the software is planned for December 2013. |
Quantity in Commerce | 148 |
Distribution | Distributed USA (nationwide) and the country of Canada. |
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 = GWN
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