RecallDepth
Class III Terminated

5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count box, Rx Only, For Spinal Anesthesia Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01

Company
Hospira Inc.
Recall Initiated
June 29, 2016
Posted
December 14, 2016
Recall Number
D-0169-2017
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
287,200 2 mL ampules
Firm Location
Lake Forest, IL, United States

Reason for Recall

Failed Stability Specifications: The recalled lots did not meet the specification for color and pH throughout shelf life.

Distribution

US and Puerto Rico

Lot / Code Info

Lot # 34-547-DK, 34-548-DK, Exp. 10/16, Lot # 39-372-DK, Exp. 03/17 Lot Number may be followed by numbers from 01 to 99

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