0.9% Sodium Chloride Injection, USP, 250 mL, Rx Only, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-7983-02
Reported: April 29, 2015 Initiated: January 20, 2015 #D-0969-2015
Product Description
0.9% Sodium Chloride Injection, USP, 250 mL, Rx Only, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-7983-02
Reason for Recall
Presence of Particulate Matter; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 661,128 containers
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
0.9% Sodium Chloride Injection, USP, 250 mL, Rx Only, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-7983-02. Recalled by Hospira Inc.. Units affected: 661,128 containers.
Why was this product recalled? ▼
Presence of Particulate Matter; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 29, 2015. Severity: Critical. Recall number: D-0969-2015.
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