Recall StatusTerminated
Date Initiated2016-11-11
Date Terminated2017-05-05
Product Quantity40,476 devices
Reason for Recall
An increase in reports indicating that the reprocessed H12LP Trocar adjustable plug may break in the packaging or during use.
Firm Action
Stryker sent an Urgent Medical Device Recall letter to all affected customers on November 11, 2016.
Customers were instructed to discontinue use of the affected lots and were asked to follow the link below to complete the Recall Effectiveness Check Form and indicate if any devices from the lots referenced in Attachment 1 remain in their inventory. This form must be completed even if no affected product is found.
www.novasyte.com/sss142
Use the following reference number as you complete the form: [Ship to Account #].
If the form indicates that any affected devices remain in your inventory, a prepaid shipping label will be issued for the return of the product. Credit for all affected devices returned will be issued to your facility.
Address any questions regarding the recall to Novasyte by calling (760) 279-3180 or emailing
[email protected].
Root Cause
No Marketing Application
Distribution Pattern
Worldwide Distribution - US (nationwide) and Internationally to Israel and Canada
Foreign distribution to the following; IL and CA
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.