Devices

Device Recall MENISCAL REPAIR NEEDLE

Model / Serial
Lot Number: 46689, 12055, 73890, 82337, 83411, 83409, 82336, 83408, 82335, 96154, 97820, 96153, 96152, 102390, 106101, 106976, 107301, 117737, and 117736.
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution -- United Arab Emirates, Austria, Australia, Belgium, Canada, Switzerland, Germany, Denmark, Spain, Finland, France, United Kingdom, Hong Kong, Ireland, Israel, India, Italy, Republic of Korea, Netherlands, Portugal, Serbia, Singapore, Slovenia, El Salvador, Thailand, Taiwan, South Africa, and throughout the U.S.
Product Description
REF 8570 MENISCAL REPAIR NEEDLE, STERILE, Rx ONLY. || CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908 USA. || Intended for use in meniscal repairs.
Manufacturer
Linvatec Corp. dba ConMed Linvatec
1 Event
- Recall of Device Recall MENISCAL REPAIR NEEDLE

Manufacturer

Linvatec Corp. dba ConMed Linvatec

Manufacturer Address
Linvatec Corp. dba ConMed Linvatec, 11311 Concept Blvd, Largo FL 33773-4908
Manufacturer Parent Company (2017)
CONMED Corp.
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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