Oxytocin 30 Units/500 mL in 0
Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
- Agency
- FDA Drug
- Recall date
- Sep 16, 2025
- Status
- Ongoing
- Company
- IntegraDose Compounding Services LLC
1. What product was recalled?
Oxytocin 30 Units/500 mL in 0
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
Quantity: 853/500 mL bags
Code or lot text: Lot #: 20250620OXY-1, Expiration date 10/18/2025
- LOT
- Expiration date 10/18/2025
- LOT
- Lot #: 20250620OXY-1
- RECALL-NUMBER
- D-0015-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Nationwide
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. The Recall Guy's urgency label is urgent, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- created
10. Where is the official source?
Open the official FDA Drug source
The Recall Guy normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.