US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 28, 2020 (6 years ago)

oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Subpotent drug - Product did not contain drug.

What was recalled

oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only, QuVa Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 888-339-0874, NDC 70092-1068-07

Recalling firm
QuVa Pharma, Inc.
NDC code
70092-1068-07
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1302-2020

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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