FDA · Drugs ·
0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers recall
Baxter Healthcare Corporation recalled 0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers on September 9, 2026 because of presence of particulate matter: Particulates identified as fiberglass. It was sold in Natonwide in the USA.
Why it was recalled
Presence of particulate matter: Particulates identified as fiberglass
What's recalled
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
Quantity: 145,464 500mL bags
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Baxter Healthcare Corporation, Deerfield, IL
- Date
- Severity
- Class I · most serious
the most serious: the product could cause serious health problems or death. - Where sold
- Natonwide in the USA
- Status
- Ongoing
- Recall number
- D-0849-2026
- Source
- U.S. Food and Drug Administration
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