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Nombre Fecha Fecha de inicio País Fuente
Retiro De Equipo (Recall) de Device Recall FlexTrayTM Endopath Bariatric Tray 2004-12-15 United States USFDA
Retiro De Equipo (Recall) de Device Recall Continuum MR Compatible Infusion Pump 2005-03-22 United States USFDA
Retiro De Equipo (Recall) de AxSYM total B-hCG Reagent is composed of one bottle of Coated Microparticles, one bottle of Alkaline Phosphatase Conjugate and one bottle of Specimen Diluent. 2005-03-24 United States USFDA
Retiro De Equipo (Recall) de Device Recall IMx Total BhCG Reagent 2005-03-24 United States USFDA
Retiro De Equipo (Recall) de Device Recall MEDPOR Surgical Implant, Catalog 6317, 20mm Sphere 2005-03-07 United States USFDA
Retiro De Equipo (Recall) de Device Recall Sequoia 2005-03-25 United States USFDA
Retiro De Equipo (Recall) de Device Recall Regius 2005-03-30 United States USFDA
Retiro De Equipo (Recall) de Device Recall Clinac 21EXS Sihlouette 2005-03-30 United States USFDA
Retiro De Equipo (Recall) de STAAR Phaco Tubing Kit 2005-03-28 United States USFDA
Retiro De Equipo (Recall) de BD 25G Spinal Needles. (Spinal Anesthesia Needle) 2005-03-16 United States USFDA
Retiro De Equipo (Recall) de Device Recall Peripherally inserted central catheter. 2005-03-25 United States USFDA
Retiro De Equipo (Recall) de Device Recall Peripherally inserted central catheter. 2005-03-25 United States USFDA
Retiro De Equipo (Recall) de Device Recall Peripherally inserted central catheter. 2005-03-25 United States USFDA
Retiro De Equipo (Recall) de Device Recall Peripherally inserted central catheter. 2005-03-25 United States USFDA
Retiro De Equipo (Recall) de Device Recall Peripherally inserted central catheter. 2005-03-25 United States USFDA
Retiro De Equipo (Recall) de Device Recall Peripherally inserted central catheter. 2005-03-25 United States USFDA
Retiro De Equipo (Recall) de Device Recall Peripherally inserted central catheter. 2005-03-25 United States USFDA
Retiro De Equipo (Recall) de Device Recall SODASORB 48 IND H MED 2005-03-31 United States USFDA
Retiro De Equipo (Recall) de Stryker brand Birthing Bed; Model 4701. 2005-03-31 United States USFDA
Retiro De Equipo (Recall) de Device Recall Perkin Elmer 2005-03-11 United States USFDA
Retiro De Equipo (Recall) de Device Recall TrepChek Syphilis Test Kit 2005-03-16 United States USFDA
Retiro De Equipo (Recall) de Device Recall FHC 2005-03-14 United States USFDA
Retiro De Equipo (Recall) de VITROS Immunodiagnostic Products TOTAL T4 REAGENT PACK, Ref #874 4468, 100 coated wells. Firm on label: Ortho-Clinical Diagnostics, Amersham UK. 2005-03-15 United States USFDA
Retiro De Equipo (Recall) de The Arrow Trerotola Percutaneous Thrombolytic Device (Product Codes: PT-65709-WC, PT-65709-W, PT-65709-HFWC, and PT-12709-WC) consists of a catheter with an expandable fragmentation basket attached to a through lumen torque cable and an outer catheter sheath. The catheter is used in conjunction with a low-speed, battery operated rotator unit to treat thrombosed hemodialysis grafts and AV fistulas. The macerating mechanism is done by 9 mm basket (made up of four stranded stainless steel wires) that rotates at 3000 rpm when rotator is activated. The current device is 7 Fr in size and comes in two lengths -- 65 cm and 120 cm. This device is used by inserting the catheter into the occluded graft or fistula via introducer sheath and then activating the rotator unit. 2005-03-18 United States USFDA
Retiro De Equipo (Recall) de Device Recall Angeion Sentinel ICD 2005-01-25 United States USFDA