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Heparin Sodium Injection Lots Recalled

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www.ProHealth.com • May 1, 2002




Wyeth Pharmaceuticals and ESI Lederle are voluntarily recalling ALL lots of Heparin Sodium Injection, USP (Porcine Derived) 1,000 units per mL, 1 mL DOSETTE ® Vial, 10 mL and 30 mL Multiple Dose Vials due to the presence of clear crystals containing an antioxidant compound from the vial rubber closures.

Read the MedWatch 2002 Safety Alert, including the "Dear Healthcare Professional" letter and FDA drug shortage information links, at: http://www.fda.gov/medwatch/SAFETY/2002/safety02.htm#hepari

Here is the FDA notice:

Heparin Sodium Injection, USP

Audience: Healthcare professionals

Wyeth Pharmaceuticals and ESI Lederle are voluntarily recalling ALL lots of Heparin Sodium Injection, USP (Porcine Derived) 1,000 units per mL, 1 mL DOSETTE ® Vial, 10 mL and 30 mL Multiple Dose Vials due to the presence of clear crystals containing an antioxidant compound from the vial rubber closures.



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