Biosite Incorporated Issues Voluntary, Nationwide Recall for Cardiac Marker Test (May

[fda.gov]

The recall is limited to the Triage Cardiac Panel, Catalog No. 97000HS, Lot No. W44467B. Biosite Incorporated has notified its customers via overnight mail and has instructed them to discontinue use of the affected lot and discard any remaining product from the lot that is on hand. The identified lot was distributed to clinical labs in the United States between January and February 2009. Replacement product will be provided to clinical labs with remaining inventory of this affected product lot.

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