Recall: D-1359-2016

Class II - Potentially Harmful

Class IIClassification

2016-06-23Initiated

TerminatedStatus

Hospira Inc.Firm

Product

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

Reason

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

Distribution

Nationwide

Source: FDA drug enforcement report via openFDA (Voluntary: Firm initiated). If you take this product, talk to your pharmacist or doctor before stopping it.