A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: MOOG Medical Devices Group, Curlin Infusion Administration Sets: Class I Recall – Potential for Reverse Flow of Fluid. According to the Food & Drug Administration FDA’s MedWatch:
Device malfunction may cause blood loss, an under-delivery of prescribed medicines or fluids, or a potential delay in therapy, leading to serious adverse health consequences, including death.
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: MOOG Medical Devices Group, Curlin Infusion Administration Sets: Class I Recall – Potential for Reverse Flow of Fluid.
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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