A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Alere Triage Diagnostic Tests (Multiple Tests): Class I Recall – Potential for Significantly Decreased Precision. According to the Food & Drug Administration FDA’s MedWatch:
Reports of patients receiving inappropriate clinical management which may have been due to erroneous test results.
For more information on the drug or medical device recall or safety alert, read the Food & Drug Administration’s FDA’s drug or medical device recall or safety alert: Alere Triage Diagnostic Tests (Multiple Tests): Class I Recall – Potential for Significantly Decreased Precision.
To report an adverse reaction, problem or other issue with a drug or medical device, submit a drug or medical device complaint to the government at fda.gov or MedWatch.
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