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DePuy Orthopaedics, Inc. recalls P.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830
Recalled September 5, 2018 · FDA recall Z-2949-2018 · DePuy Orthopaedics
Hazard
This unit may be missing the screw/collet Assembly · FDA Class II
Units
1
Sold at
The devices were not distributed in the United States. The devices were distributed to the following foreign countries: Great Britain.
Description
This unit may be missing the screw/collet Assembly
Product
P.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830
Manufacturer(s)
DePuy Orthopaedics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →