1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-4279-02
Reported: September 30, 2015 Initiated: August 25, 2015 #D-1815-2015
Product Description
1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-4279-02
Reason for Recall
Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.
Details
- Recalling Firm
- Hospira, Inc.
- Units Affected
- 100,200 Vials
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-4279-02. Recalled by Hospira, Inc.. Units affected: 100,200 Vials.
Why was this product recalled? ▼
Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 30, 2015. Severity: Moderate. Recall number: D-1815-2015.
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