US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 16, 2014 (12 years ago)

Labetalol Hydrochloride Injection, USP, 100 mg/20 mL (5 mg/mL), 20 mL Multidose Vial…

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

Why it was recalled

Presence of Particulate Matter; metal embedded in the glass vial and visible particles floating in the solution

What was recalled

Labetalol Hydrochloride Injection, USP, 100 mg/20 mL (5 mg/mL), 20 mL Multidose Vial, packaged 50/20 mL glass vials/carton, Hospira, Inc., Lake Forest, IL 60045 --- NDC 0409-2267-20

Recalling firm
Hospira Inc.
NDC code
0409-2267-20
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1424-2014

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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