Oxytocin Recall: IntegraDose IV bag 30 Units/500 mL
Announced 2026-06-24 · FDA
Oxytocin 30 Units/500 mL IV bags from IntegraDose Compounding Services LLC were recalled nationwide. Testing revealed there was no oxytocin in the bags, indicating subpotency. The recall involves 853 bags from lot 20250620OXY-1 with expiration date 10/18/2025.
| Brand | IntegraDose Compounding Services LLC |
|---|---|
| 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 | Subpotent Drug: Testing revealed there was no oxytocin in the IV bag. |
| Severity | critical |
| Units affected | 287 |
| Distribution | Nationwide in the USA |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use any remaining bags from lot 20250620OXY-1.
- Contact IntegraDose Compounding Services LLC to arrange return, replacement, or refund.
- If you have used this product, consult your prescriber or healthcare provider for guidance.
How to identify the recalled item
| Lot / date codes | Lot #: 20250620OXY-1, Expiration date 10/18/2025 |
|---|---|
| Lot / date codes | Lot#: 20260327VAS-3, BUD: 05/26/2026; 20260320VAS-3, BUD: 05/19/2026. |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.