Were You Harmed by the Baxter Heparin Syringe?
Get a free legal review when you complete the questionnaire below.
Hundreds of patients across America have fallen ill as a result of tainted
heparin syringes. If you believe you are among these unfortunate victims, our
firm may be able to assist you with your claim.
About 350 adverse events
associated with the Baxter product have been reported since the end of last year
compared to less than 100 reports in 2007, according to the Food and Drug
Administration (FDA).
Baxter Healthcare Corporation, which manufactures
Heparin, and the FDA are currently under the microscope for a recent dangerous
mix-up involving the popular blood-thinner.
Last week, news reports
revealed that the FDA had never inspected the Chinese facility that supplies the
active ingredient for Heparin.
The FDA has admitted its supplier was
never inspected because the agency confused it with another facility.
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 Drug Recall
FDA Alert: Baxter Recalls Blood-thinner Drug Heparin--Free Lawyer InfoHeparin Drug Pulled from Market--Get the Lot Numbers Recalled Here
Heparin Recall Sparks Inquiry
Congressmen: How did it happen? Probe into Heparin Recall GrowsFind out how the Heparin recall sparks congressional inquiry
heparin
Manufacture of Heparin Halted Due to Serious Allergic ReactionsHeparin Cleared For Distribution Without Safety Inspection
