Heparin Recalled

February 29, 2008 – Following two previous and smaller recalls, Baxter Healthcare has recalled all lots and doses of heparin sodium injection multi-dose and single dose vials and HEP-Lock heparin flush products.

The recalls were initiated based on numerous reports of severe allergic reactions to heparin when used during kidney dialysis.  A St. Louis doctor reported to the Centers for Disease Control that contaminated heparin was the cause.

Contaminated Chinese Heparin

Baxter Healthcare manufactures and markets heparin, a blood thinner/anticoagulant, from raw product imported from China.  In March the FDA determined that the contaminant was a chemically altered form of chondrotin sulfate.  Chondrotin sulfate is often used to treat joint pain and arthritis.  The FDA suspects that the ingredient was used an unapproved, cheap filler.

Contaminated Heparin Reactions

Reactions to the contaminated heparin are often serious and even life-threatening.  The following are possible symptoms of a contaminated heparin reaction:

• Stomach pain; nausea, vomiting, diarrhea
• Headaches
• Throat swelling
• Thirst and difficulty opening mouth
• Flushing/increased sweating
• Low blood pressure
• Chest pain/increased heartrate
• Tachycardia
• Dizziness, fainting, shortness of breath

Heparin Lawsuits

Individuals throughout the United States who required medical treatment due to a reaction to contaminated heparin may be entitled to financial compensation.  If you or a loved one have been seriously injured or a loved one has died as a result of serious reaction to heparin, please contact us immediately for a Free Case Evaluation. 

The attorneys at the Allen Law Firm are evaluating claims on behalf of individuals throughout the United States who used Heparin and suffered serious side effects requiring medical treatment. 

Contact the Allen Law Firm today for a Free Case Evaluation or call 1-888-345-LAW1.