US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 28, 2021 (5 years ago)

VANComycin 1g added to 250mL of 0.9% Sodium Chloride (Injection for Intravenous Use…

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

Why it was recalled

Crystallization: Product appears to be turbid.

What was recalled

VANComycin 1g added to 250mL of 0.9% Sodium Chloride (Injection for Intravenous Use Only), 260 mL per bag, Rx Only, This is a Compounded Drug, Hospital/Office Use Only, Apollo Care 3801 Mojave Ct, Suite 101, Columbia, MO 65202, NDC 71170-254-25

Recalling firm
Apollo Care
NDC code
71170-254-25
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0277-2022

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.

Other Chloride recalls

See all