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FDAApril 10, 2023drug

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

sca pharmaceuticalssca

UPCs

1222043028042312220430290412220430310412220430320412220430330412220430340412220430350412220430360412220430370423122204303804122204303904122204304004

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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