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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