
> Baxter Heparin Recall
Heparin, manufactured by Baxter Healthcare Corporation, has been linked to serious, life-threatening allergic reactions and death.
Heparin has been used in the United States since the 1930s. Baxter recalled nine different lots of their heparin vials on January 17, 2008. As of February 14, 2008, Baxter halted the production of all heparin multi-dose vials.
February 11, 2008 - FDA Advisory
"Baxter's Multiple-dose Vial Heparin Linked to Severe Allergic Reactions"
January 25, 2008 - FDA Advisory
"Baxter Issues Urgent Nationwide Voluntary Recall of Heparin 1,000 Units/ml 10 and 30ml Multi-Dose Vials"
The Schmidt Firm, LLP is currently accepting Heparin induced side effects claims in all 50 states. If you or somebody you know has received a Heparin injection and now suffer from a severe side effect, you should contact our firm immediately for a free case consultation. Please click here to contact our Dangerous Drug Litigation Group or call toll free 24 hours a day at 866-920-0753.
Heparin sodium is derived from pig intestines and has been marketed in the United States since the 1930s. Heparin is a blood thinner that is commonly used before certain types of surgery, including coronary artery bypass graft surgery, and in kidney patients before they undergo dialysis in order to prevent blood clots. Baxter initially recalled nine heparin lots, but problems continued, and Baxter was forced to suspend manufacturing the multi-dose vials after the FDA received reports of about 350 heparin reactions over the past 45 days. At least four deaths and hundreds of serious reactions have been reported after the use of Heparin. The heparin problems only appear to be associated with the multidose vials, and Baxter is continuing to produce the single-dose vials.
There are a variety of side effects associated with Heparin. Reactions included stomach pain or discomfort, nausea, vomiting, diarrhea, decreased or low blood pressure, chest pain, fast heart rate, dizziness, fainting, unresponsiveness, shortness of breath, feeling your heart beat strong or fast, drug ineffectiveness, burning sensation, redness or paleness of skin, abnormal sensation of the skin, mouth or lips, flushing, increased sweating, decreased skin sensitivity, headache, feeling unwell, restlessness, watery eyes, throat swelling, thirst and difficulty opening the mouth. Some of these reactions may be severe or life threatening and have led to life-threatening shock in some.
The Schmidt Firm, LLP is currently accepting Heparin induced injury cases in all 50 states. If you or somebody you know has been injured by Heparin, you should contact our firm immediately for a free case consultation. Please use the form below to contact our Dangerous Drug Litigation Group or call toll free 24 hours a day at (866) 920-0753.
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Brand Name
Heparin
Manufacturer
Baxter Healthcare Corporation
Status
Recalled
Related Content
Baxter Heparin Recall
Heparin Recall
Heparin Syringe Recall
Serratia Marcescens
Serious Side Effects
Allergic Reaction
Nausea and vomiting
Difficulty breathing
Excessive sweating
Decreased blood pressure
Shock
Infection
Death
Free Heparin Case Evaluation
Please click here to contact our Dangerous Drug Litigation Group or call toll free 24 hours a day at (866) 920-0753.
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