Devices

Euflexxa (1 sodium hyaluronate)

Model / Serial
Lot Numbers: RC0101A, Exp. 5/2010; RC0102A, Exp. 5/2010; RC0107A, Exp 5/2010; RC0114A, Exp 5/2010; RC0118A, Exp 6/2010; RC0122A, Exp 6/2010; RC0123A, Exp 6/2010; RC0127A, Exp 6/2010; and RC0131A, Exp 6/2010.
Product Classification
Orthopedic Devices
Device Class
3
Implanted device?
No
Distribution
Nationwide distribution.
Product Description
Euflexxa (1% sodium hyaluronate). Pre-filled syringe, Rx only, 3 syringes per carton; Manufactured by Ferring Pharmaceuticals In, Parsippany, NJ 07054; || Manufactured by Bio-Technology General (Israel Ltd. Be er Tuvia, Kiryat Malachi 83104 Israel. || Indicated for the treatment of pain in osteoarthritis of the knee in patients who have failed to respond adequately to conservative non-pharmacologic therapy and simple analgesics.
Manufacturer
Ferring Pharmaceuticals Inc
1 Event
- Recall of Euflexxa (1 sodium hyaluronate)

Manufacturer

Ferring Pharmaceuticals Inc

Manufacturer Address
Ferring Pharmaceuticals Inc, 4 Gatehall Dr Fl 3rd, Parsippany NJ 07054-4518
Manufacturer Parent Company (2017)
Ferring Holding S.A.
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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