RecallDepth
Class II Terminated

Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32

Company
Hospira Inc.
Recall Initiated
June 23, 2016
Posted
July 20, 2016
Recall Number
D-1359-2016
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
373,850 tubes
Firm Location
Lake Forest, IL, United States

Reason for Recall

Crystallization: Product contains particulate identified to be crystallized active ingredient.

Distribution

Nationwide

Lot / Code Info

Lot #: 52610LL, Exp. 01 OCT 2016; Lot #: 57660LL, Exp. 01 MAR 2017

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