Reported Oct 7, 2026 · Ongoing

Anticoagulant Sodium Citrate 4% w/v Solution USP, 250 mL VIAFLEX Plastic Container Product Code 2B7867Q NDC…

Baxter Healthcare Corporation

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • Anticoagulant Sodium Citrate 4% w/v Solution USP, 250 mL VIAFLEX Plastic Container Product Code 2B7867Q NDC 0338-9669-01 Strength per dose
  • dosage
    • 250mL
    • Each 100mL contains 4 g Sodium Citrate
    • USP Number of
  • units packed per shipping carton/case36
Lot codes and dates
  • Lot # Y493475
Amount recalled
415,008

Where it was sold

Why it was recalled

Stop using this product now

Baxter International Inc. is voluntarily recalling one lot of Anticoagulant Sodium Citrate Solution (Lot # Y493475) due to the potential presence of particulate matter identified as fiberglass in the solution. Intravenous administration of a blood product treated with Anticoagulant Sodium Citrate containing particulate matter may lead to adverse health consequences.

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Notice updated Oct 5, 2026 · Data as of Nov 4, 1:07 AM UTC

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