Some dialysis patients harmed by tainted heparin
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The recent mass recall of heparin has health-care providers concerned about supplies of the blood thinner that is used to clear intravenous lines and prevent clots in surgical and dialysis patients, according to the PLain Dealer newspaper on March 3, 2008.
Drugmaker Baxter International
Inc. was forced to recall vials of heparin sodium injection multidose,
single-dose vials and HEP-Lock heparin flush products after more than 400
reports of severe reactions surfaced via the Food and Drug Administration.
According to the FDA, patients experienced difficulty breathing, chest
pains, dangerous drops in blood pressure and other reactions.
An FDA
spokeswoman said 12 reports of death were associated with Baxter heparin, and
nine may or may not involve Baxter heparin.
If you were harmed after
being administered heparin, please complete the form below and a representative
of our firm will contact you as soon as possible.
see also:
Heparin Shots
Hundreds Hurt by Tainted Heparin Shots. Severe Reactions in PatientsGermany: Dangerous Allergic Reactions to Heparin Shots--Free Lawsuit
Heparin & Covidien
Heparin Maker Covidien Recalls Lots of Syringes Due to ContaminationCovidien recalls lots of filled Heparin syringes--Lawyers take cases
Heparin News, 2.28.07
Breaking News: Baxter Recalls Most Heparin Products After 4 DieHeparin Pulled From Market After News of Illness--Free Lawsuit Info


