0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare Corporation, Deerfield, IL, 60015, USA, Made in USA, NDC 0338-0049-03
Drug Recall
Official source record
- Recall number
- D-0849-2026
- Event ID
- 99678
- Classification
- Class I
- Status
- Ongoing
- Recalling company
- Baxter Healthcare Corporation
- Reason for recall
- Presence of particulate matter: Particulates identified as fiberglass
- Report date
- September 9, 2026
- Recall initiation date
- August 17, 2026
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Natonwide in the USA
Drug product identifiers
- Manufacturer
- Baxter Healthcare Corporation
- Brand name
- SODIUM CHLORIDE
- Generic name
- SODIUM CHLORIDE
- Substance name
- SODIUM CHLORIDE
- Product NDCs
- 0338-0043; 0338-0049
- Package NDCs
- 0338-0043-03; 0338-0043-04; 0338-0049-01; 0338-0049-02; 0338-0049-03; 0338-0049-04; 0338-0049-10; 0338-0049-11; 0338-0049-18; 0338-0049-31; 0338-0049-38; 0338-0049-41; 0338-0049-48
- 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.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
Where can I find more official information?
The source links below, published by the FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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.
