| Subject: | FDA Announces Recall of One Lot of Biosite Incorporated Triage Cardiac Panel |
| Category: | Food and Drug Administration (FDA)
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| Published: | Tue, 2 Jun 2009 - 01:00 pm |
| The Food and Drug Administration (FDA) and Biosite Incorporated has initiated a voluntary, nationwide recall of one lot of Triage Cardiac Panel. The test is used by healthcare professionals as an aid in the diagnosis of myocardial infarction. The product has been recalled due to reports of low recovery of quality control samples containing Creatine Kinase MB (CK-MB), troponin I and myoglobin on the affected lot. Although there have been no reported issues of patient... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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