Devices

Device Recall DePuy Mitek FMS Irrigation Intermediary Tube With Oneway Valve Arthroscopy tubing

Model / Serial
Lot Codes: 1060792 1060824 1060841 1060851 BBBA0953D BBBA0953E BBBA0953F BBBA0953G BBBA1001T BBBA1001V BBBA1002H BBBA1002I BBBA1005D BBBA1005E BBBA1005F BBBA1005G BBBA1007J BBBA1008C BBBA1008E BBBA1010G BBBA1010H BBBA1010J BBBA1010K BBBA1012B BBBA1012C BBBA1012E BBBA1014A BBBA1014E BBBA1015F BBBA1015G BBBA1018E BBBA1018F BBBA1020B BBBA1020C
Product Classification
Neurological Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution - USA (nationwide) and the coutnries of United Arab Emirates, Australia, Belgium, Switzerland, Czech, Denmark, France, UK, Italy, Netherlands, Poland, and Slovakia.
Product Description
DePuy Mitek FMS Irrigation Intermediary Tube With One-way Valve Arthroscopy tubing || Product Code: 281142 || Fluid Tissue Management
Manufacturer
DePuy Mitek, Inc., a Johnson & Johnson Co.
1 Event
- Recall of Device Recall DePuy Mitek FMS Irrigation Intermediary Tube With Oneway Valve Arthroscopy tubing

Manufacturer

DePuy Mitek, Inc., a Johnson & Johnson Co.

Manufacturer Address
DePuy Mitek, Inc., a Johnson & Johnson Co., 325 Paramount Dr, Raynham MA 02767
Manufacturer Parent Company (2017)
Johnson & Johnson
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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