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U.S. Department of Health and Human Services

Class 2 Device Recall The NAV3i Platform Power Box

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 Class 2 Device Recall The NAV3i Platform Power Boxsee related information
Date Initiated by FirmMay 13, 2014
Date PostedJune 04, 2014
Recall Status1 Terminated 3 on September 15, 2014
Recall NumberZ-1716-2014
Recall Event ID 68261
Product Classification Neurological stereotaxic Instrument - Product Code HAW
ProductThe NAV3i Platform Power Box supplies the electrical components with power (e.g. Stryker Nav3 Graphite Camera, SPC-3 Computer, IO-Tablet (touch screen) and the monitor).
Code Information Stryker Product Number: 7700-853-000 Stryker Serial Numbers: 10004
Recalling Firm/
Manufacturer		 Stryker Instruments Div. of Stryker Corporation
4100 E Milham Ave
Portage MI 49002-9704
For Additional Information Contact
269-323-7700
Manufacturer Reason
for Recall		The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and March 7, 2014 may have been assembled without electrical insulation of the soldering joints
FDA Determined
Cause 2		Process change control
ActionOn May 13, 2014, Stryker Instruments sent URGENT MEDICAL DEVICE RECALL notification to their consignees. Notification included the description of the affected product, reason for the recall, risk to health, and actions to be taken by the Customer/User. Once Stryker receives the response from the customer, a Stryker Representative will contact the customer to set up a time to perform the upgrade to the affected power box. Old Power Boxes will be returned to Stryker and placed in an industrial compactor/recycler for destruction. Questions regarding the recall are directed to Kelly Jo Whipple M-F 8am-5pm @ 269-389-2921 or kellyjo.whipple@stryker.com
Quantity in Commerce20
DistributionDistributed in the states of AR, CA, IN, LA, MA, MD, MI, MT, NV, and TX.
Total Product Life CycleTPLC 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.
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