Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1775-10
Drug Recall
Official source record
- Recall number
- D-0862-2017
- Event ID
- 77111
- Classification
- Class I
- Status
- Ongoing
- Recalling company
- Hospira Inc.
- Reason for recall
- Presence of Particulate Matter: human hair found within an internal sample syringe.
- Report date
- May 31, 2017
- Recall initiation date
- April 21, 2017
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Nationwide in the USA and Puerto Rico
Drug product identifiers
- Manufacturer
- Hospira, Inc.
- Brand name
- DEXTROSE
- Generic name
- DEXTROSE MONOHYDRATE
- Substance name
- DEXTROSE MONOHYDRATE
- Product NDC
- 0409-1775
- Package NDCs
- 0409-1775-10; 0409-1775-40
- Route
- INTRAVENOUS
Where this information comes from
View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details, or FDA Enforcement Reports versus recall announcements for why that gap exists. New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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Frequently asked questions
What does a Class I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record for what each classification level means.
Is this recall still active?
According to the FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this medication?
Do not start, stop, or change any medication based on this page. Follow the instructions published by the FDA and the recalling company (see the source links below), and talk to your pharmacist or physician if you have questions about a specific medication.
Official guidance and record verification
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Compare the medication name, manufacturer, NDC, package information, and lot number on your medication with the official FDA record to see whether it matches.
Public Health Trace last retrieved this record on July 28, 2026.
Public Health Trace republishes FDA's drug recall record and does not provide medical or medication instructions -- review the official FDA record and FDA's general drug recall guidance (linked below) for what to do.
View the official FDA record · General drug recall guidance from FDA
Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.