Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

PS-C Femoral Nonporous Rt Sz 6 Recalled by Ortho Development Corporation Due to A femoral component containing pegs was found in...

Date: April 1, 2014
Company: Ortho Development Corporation
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Ortho Development Corporation directly.

Affected Products

PS-C Femoral Nonporous Rt Sz 6, Model Number 161-1604 Component of the Balanced Knee System and Balanced Knee Revision System, for total knee arthroplasty procedures.

Quantity: 5

Why Was This Recalled?

A femoral component containing pegs was found in a box for the pegless version.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Ortho Development Corporation

Ortho Development Corporation has 8 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report