US Drug Recall Register
Class I · High risk Ongoing Initiated Sep 16, 2025 (12 months ago)

Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only…

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

Why it was recalled

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

What was recalled

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

Recalling firm
IntegraDose Compounding Services LLC
NDC code
71139-0012-1
Origin
MN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0015-2026

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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