Devices

Device Recall GENESIS(R) II, POSTERIOR STABILIZED ARTICULAR INSERT

Model / Serial
Batch No. 12GT20908
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution - USA including Nevada and Internationally to United Arab Emirates, Italy, Spain, Belgium, Bulgaria, Poland, France, Japan, Netherlands, Australia, Turkey, Russian Federation, Germany and United Kingdom.
Product Description
GENESIS(R) II, POSTERIOR STABILIZED ARTICULAR INSERT, SIZE 1-2, 13 MM QTY: (1), REF 71420806, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA || Orthopedic
Manufacturer
Smith & Nephew Inc
1 Event
- Recall of Device Recall GENESIS(R) II, POSTERIOR STABILIZED ARTICULAR INSERT

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

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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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