Lidocaine HCl Injection, USP, 2%, 20 mg per mL, packaged in 5-mL single-dose vials, 10 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL. 60045, NDC 0409-2066-05.
Reported: May 7, 2014 Initiated: December 23, 2013 #D-1278-2014
Product Description
Lidocaine HCl Injection, USP, 2%, 20 mg per mL, packaged in 5-mL single-dose vials, 10 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL. 60045, NDC 0409-2066-05.
Reason for Recall
Presence of Particulate Matter- Confimed customer complaint of particulates embedded in glass container and in contact with product solution.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 68,350 vials
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
Lidocaine HCl Injection, USP, 2%, 20 mg per mL, packaged in 5-mL single-dose vials, 10 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL. 60045, NDC 0409-2066-05.. Recalled by Hospira Inc.. Units affected: 68,350 vials.
Why was this product recalled? ▼
Presence of Particulate Matter- Confimed customer complaint of particulates embedded in glass container and in contact with product solution.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 7, 2014. Severity: Critical. Recall number: D-1278-2014.
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