Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Sep 1, 2017 (9 years ago)

Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag Rx Only

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

Why it was recalled

Subpotent Drug

Cause type: Wrong potency / content

Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.

What was recalled

Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-241-04

Affected NDC 71019-0241-04

Compare with the code on your package — it is the most precise check available.

Drug: Oxytocin

Recalling firm
Pharmedium Services, LLC
NDC code
71019-241-04
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0039-2018 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Oxytocin recalls

See all
Class III · Low risk

Oxytocin synthetic

Labeling: Not Elsewhere Classified

Terminated Labeling / mix-up Denver Solutions, LLC DBA Leiters Health NDC 71449-157-70 D-0070-2024
Class II · Moderate risk

oxyTOCIN

Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

Terminated Sterility / contamination Central Admixture Pharmacy Services, Inc. D-1134-2023

Other recalls by Pharmedium Services, LLC

All 2017 recalls