Aurobindo Pharma USA Inc. recalls Fluent Children's Fever + Pain IBUPROFEN Oral Suspension USP 100 mg per 5 mL Pain Reliever/Fever Reducer, 4 fl oz (120
Aurobindo Pharma recalls Fluent Children's Fever + Pain IBUPROFEN Oral Suspension due to missing dosing cups, which could lead to incorrect dosing for children.
Lower-risk recall
Labeling Not Elsewhere Classified: Ibuprofen Oral Suspension is missing dosing cups.
Contact the company & request your remedy
What happened, in plain English
Aurobindo Pharma is recalling Fluent Children's Fever + Pain IBUPROFEN Oral Suspension because it lacks dosing cups. This means parents might give the wrong dose to children, risking overdose or underdose. Read more at govinfonow.com/recall/36704-fluent-children-s-ibuprofen-suspension-recall-missing-dosing-cups.
Source Summary by GovInfoNow · govinfonow.com/recall/36704-fluent-children-s-ibuprofen-suspension-recall-missing-dosing-cups · Updated October 4, 2026 · FDA enforcement record: FDA #D-0065-2021
Cite this page
“Fluent Children's Ibuprofen Suspension Recall: Missing Dosing Cups.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36704-fluent-children-s-ibuprofen-suspension-recall-missing-dosing-cups. Based on FDA recall #D-0065-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0065-2021%22&limit=1).
Why it’s dangerous
The product is missing dosing cups, which are necessary for measuring the correct dose for children. Without them, parents may use the suspension without proper measurement, leading to potential underdosing or overdosing.
Who’s affected
Parents and caregivers of children using this specific ibuprofen suspension. Children are at risk of incorrect dosing if the missing dosing cups are used.
How to tell if you have this one
Check for the product name 'Fluent Children's Fever + Pain IBUPROFEN Oral Suspension USP 100 mg per 5 mL' with Berry Flavor. It was distributed by Chalkboard Health Inc. in Princeton, NJ and made in India.
- Brand
Aurobindo Pharma- Category
Drug
What to do — step by step
Check Product Label
Look for the Berry Flavor and check the NDC code 79395-003-92 on the label.
Questions people ask
Is this product safe to use?
The product is safe to use if dosing cups are available, but the recall indicates it lacks them, so it should not be used without proper measurement.
What should I do if I have this product?
The recall does not specify a remedy, so check the label for the NDC code 79395-003-92 and contact the manufacturer for guidance.
How can I tell if I have the recalled product?
Look for the Berry Flavor and NDC code 79395-003-92 on the label. The product was distributed by Chalkboard Health Inc. in Princeton, NJ.
Contact Aurobindo Pharma
We’ve drafted a message you can send Aurobindo Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0065-2021 — Aurobindo Pharma Aurobindo Pharma Hello, I own a Aurobindo Pharma that is covered by recall D-0065-2021 from Aurobindo 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-0065-2021 (October 22, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0065-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.