FDA MedWatch - Recall of CARDIAC Reader System due to falsely dec reased or false neg

  1. 0 roche 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).

    http://www.fda.gov/oc/po/firmrecalls/roche12_04.html
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    Brian has '18+' year(s) of experience and specializes in 'CCU, Geriatrics, Critical Care, Tele'. From 'Minnesota'; Joined Mar '98; Posts: 15,290; Likes: 16,230.



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