Devices

Device Recall GENESIS(R) II TIBIAL Punch

Model / Serial
15FM16181
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
International only: United Arab Emirates, Spain, Mexico
Product Description
smith&nephew; GENESIS(R) II TIBIAL Punch, 13 MM, REF 71440408, QTY: (1)
Manufacturer
Smith & Nephew, Inc.
1 Event
- Recall of Device Recall GENESIS(R) II TIBIAL Punch

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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