PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: February 4, 2015 Initiated: December 19, 2014 #Z-1032-2015

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

Reason for Recall

The lot failed pH specification.

Details

Recalling Firm
Fresenius Kabi USA, LLC
Units Affected
Domestic: 69,725
Distribution
Nationwide Distribution
Location
Lake Zurich, IL

Frequently Asked Questions

What product was recalled?
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. Recalled by Fresenius Kabi USA, LLC. Units affected: Domestic: 69,725.
Why was this product recalled?
The lot failed pH specification.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 4, 2015. Severity: Moderate. Recall number: Z-1032-2015.