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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall POSTOP EYE TRAY General and Plastic Surgery Devices Centurion Medical Products Corporation 1 United States USFDA
Device Recall Lipoplasty Solta Medical Inc United States USFDA
Device Recall ExacTrac versions 6.5 through 6.5 Radiology Devices Brainlab AG 2 United States USFDA
Device Recall VasoSeal ES Cardiovascular Devices Datascope Collagen Products Division 3 United States USFDA
DuoDecapolar Electrophysiology Catheter Cardiovascular Devices Biosense Webster, Inc. 2 United States USFDA
Progressive Medical NONSTICK CAUTERY TIP PTFE Modified Coated Blade General and Plastic Surgery Devices Progressive Medical Inc 2 United States USFDA
VITEK 2 AST P612 Biomerieux Inc United States USFDA
VITEK 2 AST GN49 Immunology and Microbiology Devices Biomerieux Inc 2 United States USFDA
VOLISTA General and Plastic Surgery Devices Maquet SAS 2 United States USFDA
Sarns brand Retrograde Cardioplegia Cannula, 17 Fr, malleable stylet, ribbed balloon, manual-inflate. Catalog # 4430 Cardiovascular Devices Terumo Cardiovascular Systems Corp 2 United States USFDA
Connection Tube Cardiovascular Devices Merit Medical Systems, Inc. 2 United States USFDA
Device Recall Arrow TwoLumen CVC Kit with Blue Flex Tip Catheter Cardiovascular Devices Arrow International Inc 2 United States USFDA
Device Recall IGS 630 Radiology Devices GE Healthcare, LLC 2 United States USFDA
Device Recall Strep A Test Card LumiQuick Diagnostics Inc. United States USFDA
Device Recall 10FR Drain Kit, Flat Full Perforated with Trocar, Saber 100ml Bulb and 3C System, Sterile (10/case) General and Plastic Surgery Devices Aspen Surgical Products, Inc. 1 United States USFDA
Device Recall Double Offset Rasp Handle, Left Hand Orthopedic Devices Zimmer, Inc. 1 United States USFDA
Device Recall ConMed Linvatech Hall Surgical Blades, Sterile ST REPEAT STERN BLADE General and Plastic Surgery Devices Linvatec Corp. 1 United States USFDA
Device Recall Koodinat M/MP Patient Table used with Multistar Radiology Devices Siemens Medical Solutions USA, Inc 2 United States USFDA
Device Recall NonVented IV Set with 2Gang "HiFlo" Stopcocks with Luer Activated HEP Lock Valves and Luer Activa General Hospital and Personal Use Devices Arrow International Inc 2 United States USFDA
Device Recall Harmony LC 500 General and Plastic Surgery Devices Steris Corporation 2 United States USFDA
Device Recall King Systems KLTD Oropharyngeal Airway Anesthesiology Devices King Systems Corp. 1 United States USFDA
Plum A Hyperbaric Single Channel Infusion Pumps General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
cobas INTEGRA 800 TinaQuant Hemoglobin A1cDX Gen.2 Clinical Chemistry and Clinical Toxicology Devices Roche Diagnostics Operations, Inc. 2 United States USFDA
Roche OMNI S Analyzer: cobas b 2216Roche OMNI S6 system Clinical Chemistry and Clinical Toxicology Devices Roche Diagnostics Operations, Inc. 2 United States USFDA
COMPLETE MultiPurpose, 10 Minute, Comfort 8 in 1, Comfort Plus, and Protec Ophthalmic Devices Advanced Medical Optics, Inc. 2 United States USFDA