Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- ...
FDA Recall #D-106-2013 — Class II — October 25, 2012
Product Description
Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01
Reason for Recall
Presence of Particulates; may contain glass particles
Recalling Firm
Hospira Inc. — Lake Forest, IL
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Drugs
Product Quantity
361,600/1-mL ampules
Distribution
Nationwide
Code Information
Lot 100953A, Exp 01OCT2013; Lot 120803A Exp 01DEC2013
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated