Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Ongoing Initiated Dec 28, 2023 (3 years ago)

PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride

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

Why it was recalled

Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

Cause type: Wrong potency / content

Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.

What was recalled

PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride (80 mcg per mL), Item F3360, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-148-94.

Affected NDC 71449-0148-94

Compare with the code on your package — it is the most precise check available.

Drug: Phenylephrine

Recalling firm
Denver Solutions, LLC DBA Leiters Health
NDC code
71449-148-94
Origin
CO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0279-2024 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week.

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