US Drug Recall Register
Class III · Low risk Terminated Initiated Nov 11, 2019 (7 years ago)

Amiodarone Hydrochloride Injection, USP, 450 mg per 9 mL (50 mg / mL), 9 mL Single Dose…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Crystallization: Presence of visible particulate matter.

What was recalled

Amiodarone Hydrochloride Injection, USP, 450 mg per 9 mL (50 mg / mL), 9 mL Single Dose Vial, Rx only, Distributed by AuroMedics Pharma LLC E. Windsor, NJ. 08520, Made in India. NDC 55150-181-09

Recalling firm
AuroMedics Pharma LLC
NDC code
55150-181-09
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0521-2020

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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