A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Medtronic Model 8637 SynchroMed II Implantable Infusion Pump: Class I Recall – Potential for Reduced Battery Performance. According to the Food & Drug Administration FDA’s MedWatch:
Potential for reduced battery performance can lead to the sudden loss of therapy and the return of underlying symptoms and/or therapy withdrawal symptoms.
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: Medtronic Model 8637 SynchroMed II Implantable Infusion Pump: Class I Recall – Potential for Reduced Battery Performance.
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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