Devices

Device Recall DePuy Mitek FMS Irrigation Intermediary Tube Without Oneway Valve Arthroscopy tubing

Model / Serial
Lot Codes: 1060790 BBBA1001N BBBA1005C BBBA1006G BBBA1014C
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 Without One-way Valve Arthroscopy tubing || Product Code: 281103 || Fluid Tissue Management
Manufacturer
DePuy Mitek, Inc., a Johnson & Johnson Co.
1 Event
- Recall of Device Recall DePuy Mitek FMS Irrigation Intermediary Tube Without 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

One device with a similar name

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Device Recall DePuy Mitek FMS Irrigation Intermediary Tube Without Oneway Valve Arthroscopy tubing

Model / Serial
Lot Codes: 1060789 1060823 1060838 1060848 1061291 1061292 BBBA1001I BBBA1003D BBBA1003E BBBA1004A BBBA1006F BBBA1007D BBBA1008A BBBA1010A BBBA1011D BBBA1014B BBBA1015R BBBA1018G BBBA1019E
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 Without One-way Valve Arthroscopy tubing (100 units/box) || (International Distribution Only) || Product Code: 281102 || Fluid Tissue Management
Manufacturer
DePuy Mitek, Inc., a Johnson & Johnson Co.

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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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