International Medical Devices Database

Manufacturer Address
Fresenius Kabi USA, LLC, 3 Corporate Dr, Lake Zurich IL 60047-8930
Manufacturer Parent Company (2017)
Fresenius SE & Co KGaA
Source
USFDA
1 Event
- Recall of Device Recall HEPFLUSH

One device in the database

Device Recall HEPFLUSH

Model / Serial
Lot 6005501, Exp. Date 1/2016
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION, USP) 100 USP units per 10 mL (10 USP units per mL), Single Dose Vial, Rx only -- Fresenius Kabi USA, LLC -- NDC 63323-017-10, Product Code 1710

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Disclaimer

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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Fresenius Kabi USA, LLC

One device in the database

Device Recall HEPFLUSH