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B. Braun Medical Recalls Lots of Heparin After Dangeorus Contaminant Found in Product

B. Braun Medical Inc. recalled 23 lots of its blood thinner on March 21, 2008 after being notified by its supplier of a nationwide recall of Heparin Sodium USP because of a contaminant, according to Reuters.

B. Braun Medical, of Irvine, California, began recalling the lots on March 21 as a precautionary measure, after Scientific Protein Laboratories said that one lot of Heparin Sodium, USP Active Pharmaceutical Ingredient it bought has a heparin-like contaminant.

The U.S. Food and Drug Administration has received reports of serious injuries and/or deaths in patients who have been administered heparin injectable products of other companies containing this contaminant.

The FDA recommends that physicians, dialysis center staff and health care providers use an alternate source of heparin or another blood-thinning drug when possible.

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.

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see also:

Heparin Lawsuits Japanese Firms Recall Heparin as Lawsuits Mount in the United States
Lawsuits Mount as People Come Forward with Heparin Related Injuries

Heparin & Surgery Blood Thinner Heparin Used in People Undergoing Heart Surgery
Millions in US Have Been Treated With Heparin During Surgery--law info

Heparin News, 2.28.07 Breaking News: Baxter Recalls Most Heparin Products After 4 Die
Heparin Pulled From Market After News of Illness--Free Lawsuit Info

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