
> Heparin Recall
There have recently been three nationwide recalls issued for different Heparin containing products manufactured by Baxter Healthcare Corporation, AM2 PAT, Inc and B. Braun / Scientific Protein Laboratories LLC.
The Schmidt Firm, LLP is currently accepting Heparin induced side effects claims in all 50 states. If you or somebody you know has been administered Heparin 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, 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.
Learn More: Baxter Heparin Recall
Pre-Filled Heparin Lock Flush Solution USP syringes used to flush intravenous and catheter lines to prevent clotting have been recalled due to the recent outbreak of blood infections associated with their use. The pre-filled syringes could be contaminated with bacteria known as Serratia marcencens. There have been close to 50 people in Texas and Illinois who have been affected by these contaminated syringes. On December 20, 2007, AM2 PAT recalled one lot of their pre-filled heparin flush syringes, 070926H. On January 25, 2008, the FDA issued a recall of all lots of heparin and saline pre-filled flush syringes.
Learn More: Heparin Syringe Recall
On March 21, 2008, B. Braun began recall the lots of heparin due to a notification received from the supplier, Scientific Protein Laboratories (SPL), disclosing that one lot of Heparin Sodium, USP Active Pharmaceutical Ingredient acquired by B. Braun Medical Inc. has a heparin-like contaminant.
Learn More: B. Braun Heparin Recall
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
B. Braun Heparin Recall
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

Brand Name
Heparin
Manufacturer
AM2 PAT, Inc., of Angier, N.C
Status
Recalled
Serious Side Effects
Sepsis
Infection
Fever
Nausea
Chills
Vomiting
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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