Devices

Device Recall Max Barrier Kit

Model / Serial
Model number: 70828, Lot number: 187176, Exp. Date: 1/1/2016.
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Distributed in the states of AR, AZ, FL, GA, IA, IL, KY, MA, MN, NC, NY, OH, TN, TX, and VA.
Product Description
Max Barrier Kit, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.
Manufacturer
Medical Action Industries Inc
1 Event
- Recall of Device Recall Max Barrier Kit

Manufacturer

Medical Action Industries Inc

Manufacturer Address
Medical Action Industries Inc, 25 Heywood Rd, Arden NC 28704-9302
Manufacturer Parent Company (2017)
Owens & Minor Inc
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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