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Zimmer, Inc. recalls Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disabling knee joint.
Recalled November 6, 2013 · FDA recall Z-0076-2014 · Zimmer
Hazard
The low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the devices. · FDA Class II
Units
32537
Sold at
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.
Description
The low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the devices.
Product
Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disabling knee joint.
Manufacturer(s)
Zimmer, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →