Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32
Reported: July 20, 2016 Initiated: June 23, 2016 #D-1359-2016
Product Description
Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32
Reason for Recall
Crystallization: Product contains particulate identified to be crystallized active ingredient.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 373,850 tubes
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32. Recalled by Hospira Inc.. Units affected: 373,850 tubes.
Why was this product recalled? ▼
Crystallization: Product contains particulate identified to be crystallized active ingredient.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 20, 2016. Severity: Moderate. Recall number: D-1359-2016.
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