FDA MedWatch: Implantable Port Recall: Smiths Medical Removes ProPort Plastic Implantable Ports Due to Manufacturing Error that May Cause Separation
FDA MedWatch: Disruptions in Availability of Hemodialysis Bloodlines
FDA MedWatch: Early Alert- Infusion Pump Issue from Baxter Healthcare Corporation
FDA MedWatch: ICU Medical Issues Nationwide Recall of Potassium Chloride Injection, 20 mEq and 10 mEq Due to Mislabeling
2744s Due March 31st, 2025!!!
FDA MedWatch: Early Alert- Infusion Pump Software Issue from Fresenius Kabi USA
FDA MedWatch-Early Alert: Solution Set Issue from Baxter Healthcare Corporation
FDA MedWatch-Early Alert: Extracorporeal Blood Circuit Issue from Nuwellis
FDA MedWatch: Astellas Pharma US, Inc. Issues Voluntary Nationwide Recall of One Lot of PROGRAF® 0.5mg (Tacrolimus) and One Lot of ASTAGRAF XL® 0.5mg (Tacrolimus Extended-Release Capsules) Because Bottles Shipped to U.S. May Contain Empty Capsules

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