Various lots of Heparin sold by B. Braun Medical Inc., manufactured in2008, have been recalled because of a trace amount of oversulfated chondroitin sulfate (OSCS) contaminant.
To file a report regarding adverse reactions to this Heparin:
• Complete and submit the report Online: www.fda.gov/MedWatch/report.htm
• Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
For further information, go to: Heparin Sodium (B. Braun): Recall - Trace Contaminant
Heparin Recalled Due to Trace Contaminant (10.29.10)
October 29, 2010
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