DePuy Orthopaedics, Inc. Recall: P.F.C. SIGMA Revision Knee System Distal Augment, Model N
DePuy Orthopaedics, Inc. Recall: P.F.C. SIGMA Revision Knee System Distal Augment, Model N is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: DePuy Orthopaedics, Inc.; Product: P.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830; Reason for recall: This unit may be missi
| Recalling firm | DePuy Orthopaedics, Inc. |
|---|---|
| Product | P.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830 |
| Reason for recall | This unit may be missing the screw/collet Assembly |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | The devices were not distributed in the United States. The devices were distributed to the following foreign countries: Great Britain. |
| Recall initiated | 20180718 |
| Recall number | Z-2949-2018 |
| Category | device |
| State | IN |
| Country | United States |
$29/mo
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