A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Maquet Medical Systems USA FLOW-i Anesthesia System: Class 1 Recall – Device Field Correction. According to the Food & Drug Administration FDA’s MedWatch:
Use of this product may cause 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: Maquet Medical Systems USA FLOW-i Anesthesia System: Class 1 Recall – Device Field Correction.
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.