A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: CareFusion Alaris PC Unit, Model 8015: Class I Recall – Error Code. According to the Food & Drug Administration FDA’s MedWatch:
Potential error code may cause a delay in patient therapy or result in serious injury and/or death to the patient.
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 PC Unit, Model 8015: Class I Recall – Error Code.
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.