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Zimmer, Inc. recalls Multipolar¿ Bipolar Cup METAL SHELL 38 MM OD through 71 MM OD. Indicated in fracture dislocation of the hip.
Recalled November 6, 2013 · FDA recall Z-0068-2014 · 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
72806
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
Multipolar¿ Bipolar Cup METAL SHELL 38 MM OD through 71 MM OD. Indicated in fracture dislocation of the hip.
Manufacturer(s)
Zimmer, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →