Map Shows States With Impacted IV As Fiberglass Detected in Saline
Summary
Baxter International recalled two lots of saline solution after finding possible fiberglass particles in the product. The contaminated saline was sent to healthcare providers in 14 states, and no patient injuries have been reported so far.Key Facts
- Baxter recalled two lots of 0.9% Sodium Chloride Injection due to possible fiberglass contamination.
- The recalled saline was distributed in 14 U.S. states between July 31 and August 3, 2024.
- The product is used for intravenous (IV) treatment and in hemodialysis.
- Fiberglass in an IV solution can cause serious health issues, including blockages in blood vessels.
- Potential risks include blood clots, organ damage, allergic reactions, and vein irritation.
- No adverse health events related to the recall have been reported as of August 25, 2024.
- Baxter is instructing customers to stop use and return the affected product.
- The FDA has been notified and is involved in managing the recall.
Read the Full Article
This is a fact-based summary from The Actual News. Click below to read the complete story directly from the original source.
