Heparin Syringe Recall Lawsuit

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B. Braun Update: 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

AM2 PAT Heparin Update: Pre-Filled Heparin Lock Flush Solution USP, manufactured by AM2 PAT, Inc., of Angier, N.C, has been linked to serious, life-threatening side effects due to contamination of Serratia marcescens.

These syringes were manufactured by Am2Pat and may be labeled as: Am2Pat, Sierra Pre-filled, or B. Braun. On December 20, 2007, AM2 PAT recalled one lot of their pre-filled heparin flush syringes. On January 25, 2008, the FDA issued a recall of all lots of heparin and saline pre-filled flush syringes.

What You Can Do & How We Can Help

The Schmidt Firm, LLP is currently accepting Sierra Pre-Filled Heparin induced side effects claims in all 50 states. If you or somebody you know has received a Sierra Pre-Filled 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.

What is the problem with Heparin?

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.

Nationwide Recall Alert - Heparin Syringe Serratia marcescens Contamination

The following links provide more information regarding the recall of the Heparin Syringe Recall and Serratia marcescens.

FDA Alert - January 25, 2008
The U.S. Food and Drug Administration (FDA) today announced a nationwide recall of all lots of heparin and saline pre-filled flush syringes manufactured by AM2 PAT, Inc., of Angier, N.C. Two lots have been found to be contaminated with Serratia marcescens, a bacterium that can cause serious injury or death.

Link to Full Article: FDA Warns Public of Contaminated Syringes

FDA Alert - December 20, 2007
AM2 PAT, Inc., Angier, North Carolina, is initiating a nationwide recall of one lot of Pre-Filled Heparin Lock Flush Solution USP (5 mL in 12 mL Syringes), Lot # 070926H. The heparin IV flush syringes have been found to be contaminated with Serratia marcescens, which have resulted in patient infections. CDC has confirmed growth of Serratia marcescens from several unopened syringes of this product.

Link to Full Article: AM2 PAT, Inc. Issues Nationwide Recall of Pre-Filled Heparin Lock Flush Solution USP (5 mL in 12 mL Syringes)

Side Effects of Heparin Induced Serratia Marcescens Infections

There are a variety of side effects associated with these contaminated syringes. The use of the syringes could cause Serratia related:

• Sepsis
  
• Infection
  
• Fever
  
• Nausea
  
• Chills
  
• Vomiting
  
• Death
  

Do I Have a Heparin Syringe Recall Lawsuit?

The Schmidt Firm, LLP is currently accepting Heparin Syringe Recall 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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