Class I · Most seriousActive recall
Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use
A reasonable chance it could cause serious harm or death.
Does this affect you?
Check your lot numberLot #: 20250620OXY-1, Expiration date 10/18/2025
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | IntegraDose Compounding Services LLC |
| NDC | 71139-0012-1 |
Show the full FDA record
| Full product label | 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 |
| Distribution | Nationwide in the USA |
| Quantity | 853/500 mL bags |
| Recall initiated | 2025-09-16 |
| Report date | 2025-10-22 |
| Recall completed | — |
| Recall number | D-0015-2026 |
| Classification | Class I |
| FDA status | Ongoing |
| Origin on file | Minneapolis MN United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.