FDA MedWatch - Recall of CARDIAC Reader System due to falsely dec reased or false neg
- 0Dec 14, '04 by brian, ADN Adminroche diagnostics announced a recall for the cardiac reader system due to
the potential for falsely decreased or false negative troponin t results and
falsely decreased myoglobin results. these tests are used as part of the
diagnostic process for myocardial infarction (heart attack).