US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 20, 2018 (9 years ago)

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

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

Why it was recalled

Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.

What was recalled

Labetalol Hydrochloride Injection, USP, 100 mg/ 20 mL (5 mg/mL), 20 mL Multidose Vial, Rx only, labeled as a) Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2267-20; and b) NOVAPLUS, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2267-25.

Recalling firm
Hospira Inc. A Pfizer Company
NDC code
0409-2267-20
Origin
KS, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0576-2018

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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