Press Releases
| Heparin Recall |
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Bloodthinner casuing adverse reactions
January 28, 2008 (Deerfield, IL) - Baxter Healthcare is recalling nine lots of heparin sodium injection 1000 units/mL 10-mL and 30-mL multidose vials from the US market due to an increase in the number of reports of adverse reactions and one possible death that may be associated with the product. Click here to read the press release from Baxter International Inc. (Read the top of the press release for the recalled lot numbers) |
Statewide Representation
