2024 Letters to Health Care Providers
The FDA posts letters to health care providers about the safe use of medical devices.
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The FDA posts letters to health care providers about the safe use of medical devices.
FDA issues a letter to health care providers on potential exposure to certain chemicals with use of GE HealthCare EVair and EVair03 compressors with certain ventilators.
Dans le traitement de la COVID-19 chez le patient non hospitalisé (poids minimal de 40 kg) qui a obtenu un résultat positif à un test de dépistage virologique direct du coronavirus 2 du syndrome respiratoire aigu sévère (SRAS-CoV-2) et qui présente un risque élevé de progression de la maladie vers une forme grave, notamment jusqu'à l'hospitalisation ou au décès.
Dans le traitement de la COVID-19 chez le patient hospitaliséâgé de 12 ans ou plus (poids minimal de 40 kg) atteint de pneumonie et ayant besoin d'oxygène d'appoint.
Omnipod 5 App recalled due to a software error which occurs when users input bolus amounts below 1 unit without adding a zero before the decimal point.
2024 Medical Device Recalls
January 5, 2024 – Englewood, Colorado, Leiters Health is voluntarily recalling 33 lots of products listed below to the user level. The recalled batches of vancomycin IV bags, phenylephrine IV bags, and fentanyl IV bags are being recalled due to the potential for superpotency because they may contain
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