PlainRecalls
FDA Drug Critical Class I Ongoing

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.

Reported: February 7, 2024 Initiated: December 28, 2023 #D-0279-2024

Product Description

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.

Reason for Recall

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

Details

Units Affected
29,016 IV bags
Distribution
Nationwide within the United States
Location
Englewood, CO

Frequently Asked Questions

What product 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.. Recalled by Denver Solutions, LLC DBA Leiters Health. Units affected: 29,016 IV bags.
Why was this product recalled?
Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 7, 2024. Severity: Critical. Recall number: D-0279-2024.