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Name Classification Manufacturer Risk Class Country Source
Device Recall EpiFix General Hospital and Personal Use Devices Merit Medical Systems, Inc 1 United States USFDA
Device Recall CADD Prizm General Hospital and Personal Use Devices Smiths Medical MD, Inc. 2 United States USFDA
Device Recall Steris QFC1728 and QFC1729 Quick Connects General Hospital and Personal Use Devices Steris Corp 2 United States USFDA
Device Recall Medfusion 3500 General Hospital and Personal Use Devices Smiths Medical MD, Inc. 2 United States USFDA
Device Recall BD General Hospital and Personal Use Devices Becton Dickinson & Company 2 United States USFDA
Device Recall Sunrise MedicalHoyer Advance Patient Lifts General Hospital and Personal Use Devices Joerns Healthcare Inc. 1 United States USFDA
Device Recall 83 Miniflex with accesory crate General Hospital and Personal Use Devices Custom Ultrasonics, Inc. 2 United States USFDA
Device Recall IMS Patient scale General Hospital and Personal Use Devices Integrated Measurement Systems, Inc. 1 United States USFDA
Device Recall Stryker stretcher General Hospital and Personal Use Devices Stryker Medical Div. of Stryker Corporation 2 United States USFDA
Device Recall Century Medium Sterilizer General Hospital and Personal Use Devices Steris Corp 2 United States USFDA
Device Recall "Shower Helper" and "Bath Helper" General Hospital and Personal Use Devices The Sisus Corporation 1 United States USFDA
Device Recall Biomet Graft Preparation System General Hospital and Personal Use Devices Biomet, Inc. 2 United States USFDA
Device Recall Biomet Graft Preparation System General Hospital and Personal Use Devices Biomet, Inc. 2 United States USFDA
Device Recall Liko Universal Sling Bar General Hospital and Personal Use Devices Liko, Inc. 1 United States USFDA
Device Recall Like Universal Sling Bar General Hospital and Personal Use Devices Liko, Inc. 1 United States USFDA
Device Recall Alaris General Hospital and Personal Use Devices Cardinal Health 303 Inc DBA Alaris Products 2 United States USFDA
Device Recall Colleague 3, 3 CX and 3 CXE Volumetric Infusion Pumps General Hospital and Personal Use Devices Baxter Healthcare Corp. 2 United States USFDA
Device Recall Baxter FloGard 6201 Volumetric Infusion Pumps General Hospital and Personal Use Devices Baxter Healthcare Corp. 2 United States USFDA
Device Recall Baxter FloGard 6301 Dual Channel Volumetric Infusion Pumps General Hospital and Personal Use Devices Baxter Healthcare Corp. 2 United States USFDA
Device Recall Embrace Enteral Pump General Hospital and Personal Use Devices Ross Products Division Abbott Laboratories 2 United States USFDA
Device Recall The Companion ClearStar Pump System General Hospital and Personal Use Devices Ross Products Division Abbott Laboratories 2 United States USFDA
Device Recall Colleague and Colleague CX Infusion Pumps General Hospital and Personal Use Devices Baxter Healthcare Corp. 2 United States USFDA
Device Recall Colleague and Colleague 3 CX Triple Channel Infusion Pumps General Hospital and Personal Use Devices Baxter Healthcare Corp. 2 United States USFDA
Device Recall Gemini, Alaris General Hospital and Personal Use Devices Cardinal Health 303 Inc DBA Alaris Products 2 United States USFDA
Device Recall PhaSeal Intravascular Administration Set General Hospital and Personal Use Devices Carmel Pharma, Inc. 2 United States USFDA