Class I

Drug Recall: Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719 Kasota Ave Se, Minneapolis, MN 55414-2842 NDC 71139-0012-1

IntegraDose Compounding Services LLC · September 16, 2025

Reason for Recall

Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.

Distribution

Nationwide in the USA

States Affected

NATIONWIDE

Quantity Affected

853/500 mL bags

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0015-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.