Mode Liste Mode Grille
Nom Date Date de mise en oeuvre Pays Source
Rappel de Device Recall Fathom"14 Steerable Guidewire Peripheral Vascular Use, 200 cm x 10 cm 2010-06-03 United States USFDA
Rappel de Device Recall Fathom"14 Steerable Guidewire, Peripheral Vascular Use, PreShaped 200 cm x 10 cm 2010-06-03 United States USFDA
Rappel de Device Recall Fathom"14 Steerable Guidewire, Peripheral Vascular Use, 300 cm x 10 cm 2010-06-03 United States USFDA
Rappel de Device Recall Fathom"14 Steerable Guidewire, Peripheral Vascular Use, PreShaped 300 cm x 10 cm 2010-06-03 United States USFDA
Rappel de Device Recall Intellivue 2010-06-28 United States USFDA
Rappel de Device Recall MEDFUSION SYRINGE INFUSION PUMP, 2010-06-22 United States USFDA
Rappel de Device Recall E.faecalis/OE PNA Fish 2010-06-08 United States USFDA
Rappel de Device Recall Temno 2010-06-25 United States USFDA
Rappel de Device Recall RM, RMAT 2010-06-11 United States USFDA
Rappel de Device Recall CLAW HEX SCREWS 2010-06-07 United States USFDA
Rappel de Device Recall MONOPLANE Xray Imaging Systems with Velara Generator 2010-02-04 United States USFDA
Rappel de Device Recall BIPLANE XRay Imaging Systems with Velara Generator 2010-02-04 United States USFDA
Rappel de Device Recall Stryker Scope Warmer 2010-06-21 United States USFDA
Rappel de Device Recall HEMOCHRON(R) HEPARIN RESPONSE TEST 2010-06-24 United States USFDA
Rappel de Device Recall QuickCat 2010-07-01 United States USFDA
Rappel de Device Recall Medtronic Carelink Monitor Model 2490C 2010-06-11 United States USFDA
Rappel de Device Recall Polycarbonate prescription single vision lenses for use in sport goggles. 2010-06-30 United States USFDA
Rappel de Device Recall Oscor PACE 203H, DualChamber External Pulse Generator 2010-06-30 United States USFDA
Rappel de Device Recall BioRad Laboratories Autoimmune EIA ANA Screening kit, 96 test 2010-06-24 United States USFDA
Rappel de Device Recall Stackhouse laser resistant suction probe 2010-05-25 United States USFDA
Rappel de Device Recall DYNASTY ACLASS POLY LINER 2010-06-07 United States USFDA
Rappel de Device Recall Rees Insulated Forceps 2010-06-25 United States USFDA
Rappel de Device Recall Hospira Accessory Power Pack 2010-07-02 United States USFDA
Rappel de Device Recall Mast Roller Pump 2010-06-18 United States USFDA
Rappel de Device Recall BCare 5 2010-06-18 United States USFDA