Home / Recalls / Medical Devices
Biomet, Inc. recalls All instrumentation associated with the Prelude PF Resurfacing Knee System.
Recalled April 13, 2016 · FDA recall Z-1318-2016 · Biomet
Hazard
Inadequate design control. · FDA Class II
Units
576
Sold at
US Distribution to the states of : CA, CO, GA, IN, KS, MI, MO, NC, NJ, OH, TN and TX.
Description
Inadequate design control.
Product
All instrumentation associated with the Prelude PF Resurfacing Knee System.
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →