A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Hospira Carpuject Pre-filled Cartridges – Drug Alert: Products May Contain More Than the Intended Fill Volume. According to the Food & Drug Administration FDA’s MedWatch:
Healthcare professionals should visually inspect and confirm that the cartridge contains the labeled fill volume before dispensing and again before administering to patients.
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 Carpuject Pre-filled Cartridges – Drug Alert: Products May Contain More Than the Intended Fill Volume.
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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