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FDA recall announcement

Anticoagulant recall 2026

Baxter International Inc. announced a recall of Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic Container. FDA lists the reason as: Potential presence of particulate matter identified as fiberglass in the solution

A specific recall was announced.

Potential presence of particulate matter identified as fiberglass in the solution

FDA publish date
August 25, 2026
Company
Baxter International Inc.
Product
Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic Container
Last checked
September 23, 2026
NDC / identifier
No specific identifier listed in this announcement
Affected lot(s)
No specific lot listed for this clarification

What the FDA announcement says

Potential presence of particulate matter identified as fiberglass in the solution

Read the original FDA recall announcement →

What to check on the package

  1. Confirm the exact product and brand name.
  2. Compare the manufacturer or distributor.
  3. Match the NDC or product identifier.
  4. Match the lot or code exactly; a drug name alone is not enough.

What to do

Compare the exact product, company, identifier, and lot with the FDA announcement. Follow the recalling company or FDA instructions for affected products.

Do not stop or change a prescribed medication based only on this page. Contact a pharmacist, prescriber, or the recalling company for instructions specific to your product.

Related FDA enforcement records

24 matching records appear in the current 24-month openFDA snapshot. Use the search tool to compare the exact manufacturer, NDC, and lot.

Search all records for Anticoagulant →

Source and limitations

This server-rendered page summarizes an FDA source and the openFDA enforcement snapshot last checked on September 23, 2026. It is not an FDA service and does not provide individual medical advice.