Stryker Howmedica Osteonics Corp.: Medical Device Recall in 2015 - (Recall #: Z-1614-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Kinemax Stem Extenders, 80 mm, Product Usage: Kinemax Cemented Stem Extenders are modular components designed to be mated with tibial baseplates or femoral components of the Modular Rotating Hinge (MRH), Scorpio Total Stabilizer (TS) or Duracon TS knee replacement systems. The Kinemax Cemented Stem Extenders are available in three different lengths, 40 mm (Part #6476-8-250), 80mm (Part #6476-8-260) and 155mm (Part #6476-8-270). The 40 mm cemented stem extender is not indicated for use in the MRH system; however, it is indicated for use with the Scorpio TS and Duracon TS systems (LRKS/G Rev. 2). Both the 80mm and 155mm stem extenders are indicated for use in all three systems.

Product Classification:

Class II

Date Initiated: February 27, 2015

Date Posted: May 20, 2015

Recall Number: Z-1614-2015

Event ID: 70784

Reason for Recall:

Stryker received four customer complaints reporting that inside the box labeled part #6476-8-260 (Kinemax Stem Extenders, 80 mm) there was a different part #6476-8-250 (Kinemax Stem Extenders, 40 mm.

Status: Terminated

Product Quantity: 4 units

Code Information:

Catalog No. 6476-8-260, Lot code: EJPLC

Distribution Pattern:

US Nationwide distribution in the states of MA and RI.

Voluntary or Mandated:

Voluntary: Firm initiated