PlainRecalls
FDA Drug Moderate Class II Terminated

Tranexamic Acid Injection USP, 1000mg/10mL, 10mL vial, Rx only. Mfd by: Fresenius Kabi USA, LLC Packaged under two labels: 1) Mfd for: APP Pharmaceuticals, LLC; Schaumburg, IL 60173, NDC 63323-563-10, and 2) Mfd in USA; for Nexus Pharmaceuticals Inc; Vernon Hills, IL 60061. NDC 14789-500-10.

Reported: January 29, 2014 Initiated: October 31, 2013 #D-1034-2014

Product Description

Tranexamic Acid Injection USP, 1000mg/10mL, 10mL vial, Rx only. Mfd by: Fresenius Kabi USA, LLC Packaged under two labels: 1) Mfd for: APP Pharmaceuticals, LLC; Schaumburg, IL 60173, NDC 63323-563-10, and 2) Mfd in USA; for Nexus Pharmaceuticals Inc; Vernon Hills, IL 60061. NDC 14789-500-10.

Reason for Recall

Presence of Particulate Matter: Particulate matter consistent with delamination of the glass vial container.

Details

Recalling Firm
Fresenius Kabi USA, LLC
Units Affected
121,456 vials
Distribution
US: Nationwide
Location
Lake Zurich, IL

Frequently Asked Questions

What product was recalled?
Tranexamic Acid Injection USP, 1000mg/10mL, 10mL vial, Rx only. Mfd by: Fresenius Kabi USA, LLC Packaged under two labels: 1) Mfd for: APP Pharmaceuticals, LLC; Schaumburg, IL 60173, NDC 63323-563-10, and 2) Mfd in USA; for Nexus Pharmaceuticals Inc; Vernon Hills, IL 60061. NDC 14789-500-10.. Recalled by Fresenius Kabi USA, LLC. Units affected: 121,456 vials.
Why was this product recalled?
Presence of Particulate Matter: Particulate matter consistent with delamination of the glass vial container.
Which agency issued this recall?
This recall was issued by the FDA Drug on January 29, 2014. Severity: Moderate. Recall number: D-1034-2014.