Devices

Device Recall GENESIS II/LEGION Resurfacing Patella with JOURNEY Peg

Model / Serial
Batch # 15GM07831
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
US Distribution to states of:FL, MO, IN and TX.
Product Description
Smith & Nephew GENESIS(R) II/LEGION(TM) PATELLAR COMPONENT, RESURFACING ROUND, 32MM STANDARD, FOR CEMENTED USE ONLY WITH JOURNEY PEG, STERILE EO, Rx only, REF Number: 71934490 || knee implant.
Manufacturer
Smith & Nephew, Inc.
1 Event
- Recall of Device Recall GENESIS II/LEGION Resurfacing Patella with JOURNEY Peg

Manufacturer

Smith & Nephew, Inc.

Manufacturer Address
Smith & Nephew, Inc., 1450 E Brooks Rd, Memphis TN 38116-1804
Manufacturer Parent Company (2017)
Smith & Nephew plc
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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