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Heparin Recall - Baxter Healthcare - Lawsuit and Lawyer

HEPARIN RECALL AND BAXTER HEALTHCARE LAWSUIT INFORMATION: Our law firm is investigating several cases involving heparin. 19 people may have died and over 700 other people may have been seriously injured by Baxter's heparin products. Prompted by adverse reactions suffered by patients given Baxter heparin products, the company initiated a recall. Baxter's heparin recall initially involved 14 lots of heparin products. The heparin recall was expanded on February 28 to include all of Baxter Healthcare's multi-dose and single-use vials of heparin sodium for injection, and their heparin lock flush solutions.

Reported adverse events have included abdominal pain, decreased blood pressure, burning sensation, chest pain, diarrhea, dizziness, drug ineffectiveness, dyspepsia, dyspnea, erythema, flushing, headache, hyperhidrosis, hypoesthesia, hypotension, increased lacrimation, loss of consciousness, malaise, nausea, pallor, palpitations, paresthesia, pharyngeal edema, restlessness, vomiting/retching, stomach discomfort, tachycardia, thirst, trismus, and unresponsiveness to stimuli. As stated above, 19 people may have died as a result of these adverse reactions associated with Baxter Healthcare heparin products.

An FDA investigation into the adverse reactions that prompted the Baxter heparin recall has found that the heparin products may have been contaminated. Read more about the investigation regarding Baxter's heparin recall.

Please do not contact us regarding heparin.

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