FDA Enforcement Class II Terminated

Stryker Orthopaedics Triathlon Femoral Distal Augment- Left; 1 single unit per package Howmedica Osteonics Corp. 325 Corporate Drive, Mahwah, NJ 07430 USA Stryker France, ZAC Satolas Green Pusignan, Av de Satoles Green 69881 Meyzieu, Cedex, France This device is used when there is a deficiency in the bone present during femoral preparation these devices are used to "fill the gap" between the implant and the bone

Recall: Z-1370-2013 · Reported May 29, 2013

Enforcement

Recall Number
Z-1370-2013
Event ID
64941
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Stryker Howmedica Osteonics Corp.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
May 29, 2013
Initiation Date
March 25, 2013
Classification Date
May 23, 2013
Termination Date
May 6, 2015
Address
325 Corporate Drive, N/A, Mahwah, NJ, 07430, United States

Description

Stryker Orthopaedics Triathlon Femoral Distal Augment- Left; 1 single unit per package Howmedica Osteonics Corp. 325 Corporate Drive, Mahwah, NJ 07430 USA Stryker France, ZAC Satolas Green Pusignan, Av de Satoles Green 69881 Meyzieu, Cedex, France This device is used when there is a deficiency in the bone present during femoral preparation these devices are used to "fill the gap" between the implant and the bone

Reason

Stryker Orthopaedics received a report that a label on the external packaging (box) of a Triathalon Femoral Distal Augment 10mm- Size 5 Left depicted a glyph of an acetabular shell rather than a femoral distal augment. In addition the label was missing a reference to the "10mm" augment thickness which per the label print is required to appear below the size reference.

Code Info

Catalog Number 5541-A-501 Lot Codes HALY, HAOO, HANG

Distribution

Nationwide distribution: USA including states of: HI, IN, MS, NC, NJ, OK, TX, and WI.

Quantity

11 units