US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Aug 25, 2015 (11 years ago)

1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.

What 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

Recalling firm
Hospira, Inc.
NDC code
0409-4279-02
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1815-2015

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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