5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01
Reported: October 9, 2013 Initiated: August 29, 2013 #D-66201-001
Product Description
5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01
Reason for Recall
Presence of Particulate Matter; report of visible particulates in the glass ampule
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 86,400 ampuls
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01. Recalled by Hospira Inc.. Units affected: 86,400 ampuls.
Why was this product recalled? ▼
Presence of Particulate Matter; report of visible particulates in the glass ampule
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 9, 2013. Severity: Moderate. Recall number: D-66201-001.
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