A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: CardioGen-82 PET Scan: Drug Safety Communication – Increased Radiation Exposure. According to the Food & Drug Administration FDA’s MedWatch:
UPDATED 01/12/2012. FDA is updating healthcare professionals and the public about preliminary findings from ongoing investigations following the voluntary recall of CardioGen-82.
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: CardioGen-82 PET Scan: Drug Safety Communication – Increased Radiation Exposure.
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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