At least five Sierra Heparin syringe lawsuits have been filed by individuals who were seriously injured by a contaminated pre-filled syringe. Thousands of Heparin pre-filled syringes and Saline pre-filled syringes have been recalled over the past thirty days after it was discovered that they could be contaminated with a bacteria which could lead to serious and potentially fatal infections. The lawyers at Saiontz & Kirk, P.A. are reviewing potential Heparin syringe lawsuits for individuals who have required medical treatment as a result of an infection after using a pre-filled syringe.
An initial recall was issued on December 20, 2007 for one lot of Sierra Pre-filled Heparin syringes which are often used at home to flush catheters and intravenous lines during the treatment of cancer and other ailments which require a long-term or permanent IV. On January 18, the syringe recall was expanded to include all pre-filled Saline and Heparin syringes manufactured by AM2 PAT, Inc., which could be sold under the brand names “Sierra Pre-Filled” or “B. Braun”.
>>PRIOR POST (1/20/2008): Saline and Heparin Pre-Filled Syringe Recall Expanded
The pre-filled syringes could be contaminated with a bacteria known as Serratia marcencens. The use of the syringes could cause Serratia related sepsis, or an infection, with symptoms including:
PRE-FILLED HEPARING SYRINGE LAWSUITS
Sierra pre-filled Heparin syringe lawsuits allege that the manufacturer negligently allowed the contaminated syringes to be sold because they did not have adequate controls in place to ensure that the syringes were sterile. An investigation by the CDC has confirmed that some of the prefilled Heparin syringes were contaminated with Serratia marcescens, and an FDA inspection of the facility where the pre-filled syringes were made found that the manufacturer was not in compliance with federal regulations.
If you, a friend or family member have experienced problems after using a B. Braun or Sierra Pre-filled Heparin or Saline syringe, request a free claim evaluation.