CareFusion Alaris Pump Module Model 8100: Class I Recall – Motor Stalls During Infusion

by admin on August 26, 2012

A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: CareFusion Alaris Pump Module Model 8100: Class I Recall – Motor Stalls During Infusion. According to the Food & Drug Administration FDA’s MedWatch:

Motor stalls could result in a termination of infusion.

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: CareFusion Alaris Pump Module Model 8100: Class I Recall – Motor Stalls During Infusion.

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.

If you have thoughts on the drug or medical device recall or safety alert, share your drug or medical device recall or safety alert comments below.

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