US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 11, 2021 (5 years ago)

Phenylephrine HCl Injection, USP, 10 mg per mL, 1 mL per Single-Dose Vial packaged in 25…

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

Why it was recalled

Lack of Assurance of Sterility: customer complaints of loose crimped vial overseals which may result in a non-sterile product.

What was recalled

Phenylephrine HCl Injection, USP, 10 mg per mL, 1 mL per Single-Dose Vial packaged in 25 x 1 mL Single-Dose Vials per carton, For Intravenous Use, Rx only, Mfd. for: SAGENT Pharmaceuticals, Schaumburg, IL 60195; Made in India, NDC: 25021-315-01.

Recalling firm
Sagent Pharmaceuticals Inc
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0305-2021

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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