QuVa Pharma, Inc. recalls oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only, QuVa Pharma 1075
QuVa Pharma recalls oxyTOCIN 30 Units/500 mL IV solution (NDC 70092-1068-07) due to subpotent drug content. This means the product does not contain the required medication. Affected units were manufactured on Lot #30010515.
Lower-risk recall
Subpotent drug - Product did not contain drug.
Contact the company & request your remedy
What happened, in plain English
QuVa Pharma is recalling oxyTOCIN 30 Units/500 mL IV solutions because they contain less medication than labeled. This means the product may not work as intended when used for medical purposes. Read more at govinfonow.com/recall/37093-quva-pharma-oxytocin-30-units-5-000-ml-iv-solution.
Source Summary by GovInfoNow · govinfonow.com/recall/37093-quva-pharma-oxytocin-30-units-5-000-ml-iv-solution · Updated October 5, 2026 · FDA enforcement record: FDA #D-1302-2020
Cite this page
“QuVa Pharma oxyTOCIN 30 Units/5:000 mL IV Solution Recall: Subpotent Drug.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37093-quva-pharma-oxytocin-30-units-5-000-ml-iv-solution. Based on FDA recall #D-1302-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1302-2020%22&limit=1).
Why it’s dangerous
The product contains less medication than labeled, so it may not provide the intended medical effect. This could lead to ineffective treatment if used as prescribed.
Who’s affected
Patients prescribed oxyTOCIN 30 Units/500 mL IV solutions by a healthcare provider. Those who received the product with Lot #30010515 are most at risk.
How to tell if you have this one
Check the product label for 'oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only'. Look for Lot #30010515 on the packaging.
- Brand
QuVa Pharma- Category
Drug
What to do — step by step
Check Product Label
Look for the lot number 30010515 on the packaging to confirm if it's affected.
Questions people ask
Is this product safe to use?
No, the product may not contain the required medication, so it could be ineffective for medical use.
How can I tell if I have the recalled product?
Check the product label for 'oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only' and Lot #30010515.
What should I do if I have the recalled product?
The recall record does not specify a remedy, so contact your healthcare provider for guidance.
Contact QuVa Pharma
We’ve drafted a message you can send QuVa Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-1302-2020 — QuVa Pharma QuVa Pharma Hello, I own a QuVa Pharma that is covered by recall D-1302-2020 from QuVa Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1302-2020 (May 28, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1302-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.