Contaminated Heparin Lawyers

Contaminated Heparin in Association with Medical Devices- In an investigation following a February 2008 recall of heparin sodium for injection, the Food and Drug Administration (FDA) identified a previously unknown contaminant in the blood-thinning drug. In a follow-up July 2008 advisory, the FDA revealed that contaminated heparin had also been found in association with certain medical devices, some of which had also been recalled. The FDA is continuing to investigate the situation.

Heparin is an anticoagulant (blood thinner) that makes an anti-clotting protein in the body work better, and is usually given before certain types of surgery to prevent and treat blood clots in arteries, veins, and the lungs. Certain medical devices and diagnostic products contain, are coated with, and/or are manufactured using heparin. Some of the devices that may be affected by the heparin contamination include:

* Heparin solutions in pre-filled syringes and lock flush solutions in vials
* Certain filters, oxygenators, cannulae, and reservoirs used in cardiopulmonary bypass procedures
* Certain vascular access, retransfusion, drainage and thermodilution catheters and oximetry probes
* Certain vascular grafts and stents
* Some assisted reproduction media devices
* Certain In-Vitro Diagnostic media (IVDs) and related devices