US Drug Recall Register
Class I · High risk Completed Initiated Apr 29, 2024 (2 years ago)

Phenylephrine in 0.9% Sodium Chloride Injection Preservative Free, 100mcg/mL, 5mL…

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

Why it was recalled

Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.

What was recalled

Phenylephrine in 0.9% Sodium Chloride Injection Preservative Free, 100mcg/mL, 5mL syringe, Rx only, Hikma Injectables USA Inc, 36 Stults Road, Dayton, NJ 08810, NDC 63037-123-25

Recalling firm
Hikma Injectables USA Inc
NDC code
63037-123-25
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0508-2024

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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