Devices

Device Recall LEGION Pressfit Stem

Model / Serial
Lot Number: 06DM08612.
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution -- US, Canada, Australia, Germany, GB, Italy, Switzerland, Spain, and France.
Product Description
LEGION Pressfit Stem, Straight, 20 MM X 160 MM, REF 71424053, Sterile, Smith & Nephew, Memphis TX 38116. || The device is used for Orthopedic Knee Implants.
Manufacturer
Smith & Nephew Inc
1 Event
- Recall of Device Recall LEGION Pressfit Stem

Manufacturer

Smith & Nephew Inc

Manufacturer Address
Smith & Nephew Inc, 1450 E. Brooks Rd, Memphis TN 38116
Manufacturer Parent Company (2017)
Smith & Nephew plc
Source
USFDA

One device with a similar name

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Device Recall LEGION Pressfit Stem

Model / Serial
Lot Number: 06DAB0023.
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution -- US, Canada, Australia, Germany, GB, Italy, Switzerland, Spain, and France.
Product Description
LEGION Pressfit Stem, Straight, 10 MM X 160 MM, REF 71424043, Sterile, Smith & Nephew, Memphis TX 38116. || The device is used for Orthopedic Knee Implants.
Manufacturer
Smith & Nephew Inc

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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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