A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Hospira Symbiq Infusion System Touchscreen: Class 1 Recall – May Not Respond to Selection. According to the Food & Drug Administration FDA’s MedWatch:
Failure of touchscreen to respond to user input could result in a delay or interruption in therapy or over delivery or under delivery of medication.
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: Hospira Symbiq Infusion System Touchscreen: Class 1 Recall – May Not Respond to Selection.
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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