FDA recall D-0015-2026

Product

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

Reason for recall

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

Distribution

Nationwide in the USA

Key facts

Status

Ongoing

Initiation date

2025-09-16

Report date

2025-10-22

Voluntary/Mandated

Voluntary: Firm initiated

Location

Minneapolis, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0015-2026