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FDAFDA · Food and drugs·Recall number Z-0078-2014

Natural-Knee¿ II Femoral Component

Published November 6, 2013 · Recall initiated: August 30, 2013

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

The low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the devices.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Zimmer, Inc.
Distributor
Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Dominican Republic, Ecuador, El Salvador, Germany, Guatemala, Honduras, Hong Kong, India, Israel, Jamaica, Japan, Korea, Malaysia, Mexico, New Zealand, Nicaragua, Panama, Peru, Singapore, Taiwan, Thailand, and Venezula.
Lot
Part Number Range:6212, 6307-00-006/051
Risk classification
Class II
Area (FDA)
device
Country
United States

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