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FDA Classifies Insulet Omnipod Recall as Serious After Injury Reports
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기사 요약
FDA classified Insulet's Omnipod pod recall as Class I after reports of insulin under-delivery linked to 24 serious injuries.
기사 원문에서 발췌했어요.뉴스 본문을 불러오고 있어요.
FDA classified Insulet's Omnipod pod recall as Class I after reports of insulin under-delivery linked to 24 serious injuries.
기사 원문에서 발췌했어요.
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