Devices

Device Recall ARHTROSCOPY PK L/F

Model / Serial
Code: 900982 Lots: 141015603 exp. 10/31/15 141216365 exp. 12/31/15 150116540 exp. 1/31/16 150116982 exp. 1/31/16 150418429 exp. 5/31/16 150317871 exp. 5/31/16 150518850 exp. 6/30/16
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Distributed Only in Puerto Rico.
Product Description
ARTHROSCOPY PK L/F 5/CS || Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate
Manufacturer
Customed, Inc
1 Event
- Recall of Device Recall ARHTROSCOPY PK L/F

Manufacturer

Customed, Inc

Manufacturer Address
Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
Manufacturer Parent Company (2017)
Customed 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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