US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 29, 2013 (13 years ago)

5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only…

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

Why it was recalled

Presence of Particulate Matter; report of visible particulates in the glass ampule

What 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

Recalling firm
Hospira Inc.
NDC code
0409-4712-01
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-66201-001

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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