PlainRecalls
FDA Drug Critical Class I Terminated

0.25% Bupivacaine HCl Injection, USP, 2.5 mg/mL, 30 mL, Single-dose, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1159-02

Reported: December 25, 2013 Initiated: July 12, 2013 #D-380-2014

Product Description

0.25% Bupivacaine HCl Injection, USP, 2.5 mg/mL, 30 mL, Single-dose, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1159-02

Reason for Recall

Presence of particulate matter: visible free floating and partially embedded particulate matter in the glass vials.

Details

Recalling Firm
Hospira Inc.
Units Affected
118,100 vials
Distribution
Nationwide
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
0.25% Bupivacaine HCl Injection, USP, 2.5 mg/mL, 30 mL, Single-dose, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1159-02. Recalled by Hospira Inc.. Units affected: 118,100 vials.
Why was this product recalled?
Presence of particulate matter: visible free floating and partially embedded particulate matter in the glass vials.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 25, 2013. Severity: Critical. Recall number: D-380-2014.