US Drug Recall Register
Class I · High risk Terminated Initiated Dec 23, 2013 (13 years ago)

Lidocaine HCl Injection, USP, 2%, 20 mg per mL, packaged in 5-mL single-dose vials, 10…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Particulate Matter- Confimed customer complaint of particulates embedded in glass container and in contact with product solution.

What 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.

Recalling firm
Hospira Inc.
NDC code
0409-2066-05
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1278-2014

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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