0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-02
Reported: June 26, 2013 Initiated: June 6, 2013 #D-608-2013
Product Description
0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-02
Reason for Recall
Lack of Assurance of Sterility: The product has the potential for solution to leak at or near the administrative port of the primary container.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 676,872 containers
- Distribution
- Nationwide and Puerto Rico
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-02. Recalled by Hospira Inc.. Units affected: 676,872 containers.
Why was this product recalled? ▼
Lack of Assurance of Sterility: The product has the potential for solution to leak at or near the administrative port of the primary container.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 26, 2013. Severity: Moderate. Recall number: D-608-2013.
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