A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Stryker Wingspan Stent System: Safety Communication – Narrowed Indications for Use. According to the Food & Drug Administration FDA’s MedWatch:
Wingspan may present unacceptable risks, such as stroke and death, to many patients previously considered appropriate for treatment with Wingspan.
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: Stryker Wingspan Stent System: Safety Communication – Narrowed Indications for Use.
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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