Device Recall OrthoTec

Model / Serial
Lots 03082022, 03082042, 0308102, 03082122, 03082162, 03082202, 03082222, 03092242, 03092302, 03092322, 03092342, 03092402, 03092422, 03092442 and 03092462.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
United States, France and United Kingdom.
Product Description
Stryker brand OrthoTec pulsed irrigation/suction handpiece and tubing set; part number 0203-020-000.
Manufacturer
Stryker Instruments, Instruments Div.
1 Event
- Recall of Device Recall OrthoTec

Manufacturer

Stryker Instruments, Instruments Div.

Manufacturer Address
Stryker Instruments, Instruments Div., 4100 E. Milham, Kalamazoo MI 49001
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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