QuVa Pharma, Inc. recalls Norepinephrine 8 mg (32 mcg/mL) added to 0.9% Sodium Chloride Injection 250 mL Bag, Rx only, Compounded by: QuVA Pharma
QuVa Pharma recalls norepinephrine injection compounded with 5% dextrose instead of 0.9% sodium chloride. This may cause incorrect dosing. Contact for details.
Lower-risk recall
Incorrect excipient: Product was compounded in 250 mL 5% Dextrose instead of 250 mL 0.9% Sodium Chloride
Contact the company & request your remedy
What happened, in plain English
QuVa Pharma recalled norepinephrine injection that was compounded with 5% dextrose instead of 0.9% sodium chloride. This could lead to incorrect dosing if used as intended. Read more at govinfonow.com/recall/39414-quva-pharma-norepinephrine-injection-recall-incorrect-compounding-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/39414-quva-pharma-norepinephrine-injection-recall-incorrect-compounding-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0295-2019
Cite this page
“QuVa Pharma Norepinephrine Injection Recall: Incorrect Compounding Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39414-quva-pharma-norepinephrine-injection-recall-incorrect-compounding-risk. Based on FDA recall #D-0295-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0295-2019%22&limit=1).
Why it’s dangerous
The product was compounded using 5% dextrose instead of 0.9% sodium chloride. This incorrect excipient could lead to incorrect dosing if the injection is used as intended.
Who’s affected
Prescription patients who received this specific compounded norepinephrine injection. Healthcare providers using the product for medical treatment are at risk.
How to tell if you have this one
Check for product code 70092-9035-05 and lot number 10016014. The product was sold by QuVa Pharma in Sugar Land, TX.
- Brand
QuVa Pharma- Category
Drug
What to do — step by step
Check Product Details
Verify the product code (70092-9035-05) and lot number (10016014) on the injection label.
Questions people ask
Is this product safe to use?
The recall indicates a potential dosing error due to incorrect compounding. Do not use until confirmed safe.
What should I do if I have this product?
The recall does not specify a remedy. Check product details and contact QuVa Pharma for guidance.
How can I confirm if I have the recalled product?
Look for product code 70092-9035-05 and lot number 10016014 on the injection label.
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-0295-2019 — QuVa Pharma QuVa Pharma Hello, I own a QuVa Pharma that is covered by recall D-0295-2019 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-0295-2019 (November 21, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0295-2019 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.