A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Mizuho OSI Modular Table Systems: Class I Recall – Reports of Patient Injury. According to the Food & Drug Administration FDA’s MedWatch:
Potential for patient falls or unanticipated patient movement, which may result in serious injury or 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: Mizuho OSI Modular Table Systems: Class I Recall – Reports of Patient Injury.
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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