Devices

Device Recall ProLite Mesh

Model / Serial
Product Code/REF 1010306-06 Lot Number/LOT: 412298
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
Yes
Distribution
Internationally to Spain only.
Product Description
ProLite Mesh - mesh, surgical, polymeric || ProLite Mesh is intended for use in soft tissue deficiencies including hernia repair, traumatic or surgical wounds and chest wall reconstruction procedures requiring reinforcement with a non-absorbable supportive material.
Manufacturer
Atrium Medical Corporation
1 Event
- Recall of Device Recall ProLite Mesh

Manufacturer

Atrium Medical Corporation

Manufacturer Address
Atrium Medical Corporation, 40 Continental Blvd, Merrimack NH 03054-4332
Manufacturer Parent Company (2017)
Getinge AB
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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