US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 10, 2023 (3 years ago)

Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL, Rx Only, Single Dose Container…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent Drug: Out of specification results for low potency was obtained.

What was recalled

Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL, Rx Only, Single Dose Container, SCA Pharmaceuticals, Windsor, CT 06095, NDC# 70004-085-44

Recalling firm
SCA Pharmaceuticals
NDC code
70004-085-44
Origin
CT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0555-2023

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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