Baxter 70% Dextrose Injection, USP in 2000 mL VIAFLEX Plastic Container
OFFICIAL-SOURCE RECALL · UNITED STATES
Baxter 0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic Recall: Potential presence of particulate
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CountryUnited StatesPublishedAugust 26, 2026Last updatedAugust 26, 2026Official source last checkedAugust 27, 2026 at 2:36 PM UTC
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- Baxter
- Product
- 0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic Container
- Manufacturer
- Baxter International Inc.
- NDC
- 0338-0049-03
- Lot number
- Y495523
- Expiration date
- 31-Oct-2027
- Package size
- 500 mL
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
Potential presence of particulate matter identified as fiberglass in the solution.
Hazard
Potential presence of particulate matter identified as fiberglass in the solution.
What consumers should do
Consumers with questions regarding this recall can contact Baxter Healthcare Center for Service at 888-229-0001 between the hours of 7:00 am and 6:00 pm Central Time, Monday through Friday. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Official recall notice
Baxter Issues Voluntary Nationwide Recall for Two Lots of 0.9% Sodium Chloride Injection Due to Potential Presence of Particulate Matter
Agency: U.S. Food & Drug Administration
Official publication date: August 26, 2026
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