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
Manufacturer
Fresenius Kabi USA, LLC
1 Event
- Recall of Device Recall HEPFLUSH

Manufacturer

Fresenius Kabi USA, LLC

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

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