Devices

Device Recall GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL

Model / Serial
Lot Number 12LM03798
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
International only: Germany, France, United Arab Emirates, and United Kingdom.
Product Description
GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL, SIZE 3-4, A/P 48 MM, M/L 68 MM, QTY 1, NON-STERILE, REF 71430490, || Product Usage: || Orthopedic
Manufacturer
Smith & Nephew Inc
1 Event
- Recall of Device Recall GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL

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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