Devices

Device Recall SmartSeal Wedge Femoral Pressuriser

Model / Serial
All lots.
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution -- including States of Arkansas, California, Colorado, Florida, Idaho, Illinois, Indiana, Kentucky, Maine, Michigan, Mississippi, New Mexico, North Carolina, Pennsylvania, South Dakota, Texas, Utah and Washington.
Product Description
SmartSeal Wedge Femoral Pressuriser; Product Code/Catalog No: 3206002, DePuy Orthopaedics, Inc., 700 Orthopaedics Drive, Warsaw, Indiana 46581-0988-This product allows for effective and controlled pressurization of bone cement into the femur and the acetabulum during hip arthroplasty procedures
Manufacturer
Depuy Orthopaedics, Inc.
1 Event
- Recall of Device Recall SmartSeal Wedge Femoral Pressuriser

Manufacturer

Depuy Orthopaedics, Inc.

Manufacturer Address
Depuy Orthopaedics, Inc., 700 Orthopaedic Dr, Warsaw IN 46582-3994
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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