Mode Liste Mode Grille
Nom Date Date de mise en oeuvre Pays Source
Rappel de Device Recall Surgical Instrument for SMR Anatomic and Reverse Shoulder Prosthesis 2016-07-21 United States USFDA
Rappel de Device Recall Light Adaptor for SBD & SBD II 2016-06-24 United States USFDA
Rappel de Device Recall FPS 35mm x 3.5 mm nonlocking screw 2016-07-21 United States USFDA
Rappel de Device Recall RESPONSIVE, KNEE: FEMORAL COMPONENT CR/CS, SIZE 3R, REF 90SRK311300 2016-07-18 United States USFDA
Rappel de Device Recall RESPONSIVE, KNEE: FEMORAL total knee replacement COMPONENT CR/CS, SIZE 4R, REF 90SRK311400 2016-07-18 United States USFDA
Rappel de Device Recall RESPONSIVE, KNEE: FEMORAL COMPONENT CR/CS, SIZE 5R, REF 90SRK311500 2016-07-18 United States USFDA
Rappel de Device Recall RESPONSIVE, KNEE: FEMORAL COMPONENT CR/CS, SIZE 3L, REF 90SRK312300 2016-07-18 United States USFDA
Rappel de Device Recall TIBIAL TRAY , SIZE 2, REF 90SRK200200 2016-07-18 United States USFDA
Rappel de Device Recall TIBIAL TRAY , SIZE 3, REF 90SRK200300 2016-07-18 United States USFDA
Rappel de Device Recall TIBIAL TRAY , SIZE 4, REF 90SRK200400 2016-07-18 United States USFDA
Rappel de Device Recall TIBIAL TRAY , SIZE 5, REF 90SRK200500 2016-07-18 United States USFDA
Rappel de Device Recall Integra 2016-07-21 United States USFDA
Rappel de Device Recall Adaptor for SBD II 2016-06-24 United States USFDA
Rappel de Device Recall Procotyl (Rim Lock) Liners 2016-06-21 United States USFDA
Rappel de Device Recall Stryker AccuLIF PL Cages 2016-07-26 United States USFDA
Rappel de Device Recall Dynasty Liners 2016-06-21 United States USFDA
Rappel de Device Recall Stryker AccuLIF PL Cages 2016-07-26 United States USFDA
Rappel de Device Recall Stryker AccuLIF PL Cages 2016-07-26 United States USFDA
Rappel de Device Recall 3.5mm Bowed Locking Compression Femur Plates 2016-07-27 United States USFDA
Rappel de Device Recall 3.5mm Bowed Locking Compression Femur Plates 2016-07-27 United States USFDA
Rappel de Device Recall Lineage Liners 2016-06-21 United States USFDA
Rappel de Device Recall ROIA Anterior Delivery Device 2016-08-29 United States USFDA
Rappel de Device Recall Trident Universal Impactor/Positioner 2016-08-18 United States USFDA
Rappel de Device Recall TriMed SemiTubular Plate 2016-08-29 United States USFDA
Rappel de Device Recall Lineage Shell 2016-06-21 United States USFDA