FDA Recall Terminated

SwishTapered Implant

Recall: Z-1112-2017 · Initiated December 12, 2016

Recall

Recall Number
Z-1112-2017
Event Number
76111
Firm
Implant Direct Sybron Manufacturing, LLC
FEI Number
3001617766
Product Code
DZE
Status
Terminated
Root Cause
Packaging process control
Initiated
December 12, 2016
Posted
January 28, 2017
Terminated
May 22, 2017
Address
3050 E Hillcrest Dr, Westlake Village, CA, 91362-3171

Description

SwishTapered Implant

Reason

The extender product code (9037-03) that is packaged with the SwishTapered (Part Number 933308; Lot Number 73241) Implant was packaged in the incorrect position. This discrepancy may lead to the possibility of extender not seating properly on the implant, which may lead to micro-leakage and a possible infection to the patient.

Action

Customer notification letters were sent on 12/12/16. Customers were requested to review inventory for the affected product. Complete and return the Acknowledgement and Recall Return Form within 48 hours. If customers are an authorized distributor the firm requests that they identify those customers that may have been shipped the affected product lot and contact those customers to inform them of the issue within 48 hours of receipt of the notification in order to provide the customers with replacement product. If customers have any of the affected product the firm will send a replacement part. Any questions contact Implant Direct Sybron Manufacturing LLC Customer Care at 1-888-649-6425.

Distribution

U.S. distribution to the following; NM, TX, CA, OR, OH, ME. Foreign distribution to the following; Netherlands.

Quantity

17