• Acerca de la base de datos
  • ¿Cómo usar la IMDD?
  • Descargar la data
  • Preguntas frecuentes
  • Créditos
Vista de la lista Vista de las tarjetas
  • Dispositivo 988
  • Fabricante 214
  • Evento 124969
  • Implante 233
Device Recall Coblator II System
  • Modelo / Serial
    Serial Numbers: CA0N0000FT, CA0N0000H0, CA0N0000H7, CA0N0000J6, CA0N0000KJ, CA0N0000KK, CA0N0000KL, CA0N0000FW, CA0N0000G5, CA0N0000G6, CA0N0000H1, CA0N0000FR, CA0N0000FZ, CA0N0000KF, CA0N0000GH
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution in the states of TN, IA, AZ, NE, SD, NY, and OK.
  • Descripción del producto
    Coblator II System, 120V. || Product Usage: The Coblator II (Model RF8000E) is a bipolar, radiofrequency electrosurgical system designed for use in otorhinolaryngology (ENT) surgery. The system consists of the following components: an electrosurgical radiofrequency controller, a reusable, non-sterile Power Cord; a reusable, non-sterile Foot Control; a reusable, non-sterile Flow control Valve Unit; a reusable, non-sterile flow control cable; a single use, disposable, sterile Wand. The Coblator II is indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorhinolaryngology (ENT) surgery.
  • Manufacturer
    ArthroCare Medical Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Coblator II System
Device Recall EVac 70 XTRA with Integrated Cable
  • Modelo / Serial
    Lot Numbers: 1092289, 1092288, 1092287, 1092284, 1092276, 1085237 (Expiration date: 09JAN2017)
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution
  • Descripción del producto
    EVAC 70 XTRA with Integrated Cable REF EICA5872-01 || Product Usage: || PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorhinolaryngology (ENT) surgery including: adenoidectomy, cysts, head, neck, oral, and sinus surgery, mastoidectomy, myringotomy with effective hemorrhage control, nasal airway obstruction by reduction of hypertrophic nasal turbinates, nasopharyngeal/laryngeal indications including tracheal procedures, laryngeal polypectomy, and laryngeal lesion debulking, neck mass, papilloma keloids, submucosal palatal shrinkage, submucosal tissue shrinkage, tonsillectomy (including palatine tonsils), traditional uvulopalatoplasty (RAUP), tumors, and tissue in the uvula/soft palate for the treatment of snoring. It is intended for procedures using a conductive media, such as normal saline or Ringers lactate.
  • Manufacturer
    ArthroCare Medical Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall EVac 70 XTRA with Integrated Cable
Device Recall PROcise XP Wand with Integrated Cable
  • Modelo / Serial
    Lot Numbers: 1092290, 1092291, 1092292
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution
  • Descripción del producto
    PROcise XP Wand with Integrated Cable REF EICA8872-01 || Product Usage: || PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorhinolaryngology (ENT) surgery including: adenoidectomy, cysts, head, neck, oral, and sinus surgery, mastoidectomy, myringotomy with effective hemorrhage control, nasal airway obstruction by reduction of hypertrophic nasal turbinates, nasopharyngeal/laryngeal indications including tracheal procedures, laryngeal polypectomy, and laryngeal lesion debulking, neck mass, papilloma keloids, submucosal palatal shrinkage, submucosal tissue shrinkage, tonsillectomy (including palatine tonsils), traditional uvulopalatoplasty (RAUP), tumors, and tissue in the uvula/soft palate for the treatment of snoring. It is intended for procedures using a conductive media, such as normal saline or Ringers lactate.
  • Manufacturer
    ArthroCare Medical Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall PROcise XP Wand with Integrated Cable
Device Recall EVac 70 XTRA with Integrated Cable and PROcise EZ View with Integrated Cable
  • Modelo / Serial
    Lot numbers 1093290 and 1091254
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US Nationwide and the countries of Australia, Belgium, Germany, Spain, United Kingdom, Ireland, India, Italy and Singapore.
  • Descripción del producto
    EVac 70 XTRA with Integrated Cable and PROcise EZ View with Integrated Cable || Product Usage: || PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorhinolaryngology (ENT) surgery including: adenoidectomy, cysts, head, neck, oral, and sinus surgery, mastoidectomy, myringotomy with effective hemorrhage control, nasal airway obstruction be reduction of hypertrophic nasal turbinates, nasopharyngeal/laryngeal indications including tracheal procedures, laryngeal polypectomy, and laryngeal lesion debulking, neck mass, papilloma keloids, submucosal palatal shrinkage, submucosal tissue shrinkage, tonsillectomy (including palatine tonsils), traditional uvulopalatoplasty (RAUP), tumors, and tissue in the uvula/soft palate for the treatment of snoring. It is intended for procedures using a conductive media, such as normal saline or Ringers lactate.
  • Manufacturer
    ArthroCare Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall EVac 70 XTRA with Integrated Cable and PROcise EZ View with Integrated Cable
Device Recall smith & nephew
  • Modelo / Serial
    50209581 50220887 50231401 50216929 50226220 50231932 50218285 50229266 50235063 50240019 50245683 50251109 50254562 50256942 50263784 50279382 50291593 50302984 50303418 50327069 50330377 50351345 50361381 50404796 50408768 50419699 50433964 50250837 50256854 50269580 5027766 50304642 50342002 50401593 50417254
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- US, including the states of AL, AR, CA, FL, GA, ID, IL, KS, MA, MI, MO, NC, TN, TX, and AK; and, country of Japan.
  • Descripción del producto
    High Flow Irrigation Extender; Part Number 72201021. || Arthroscopic accessories are indicated for use in access of the joint capsule.
  • Manufacturer
    Smith & Nephew, Inc., Endoscopy Div.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall smith & nephew
Device Recall Smith & Nephew
  • Modelo / Serial
    Lot Codes: ( Devices within Expiry) 3009063 3009559 3010117 3010720 3011688 3012095 3012366 3014560 3016455 3018390 3020194 3022929 3025736 3027818 3030178 3032892 3036529 3071312 3071546 3074279 3074280 3076377 3076427 3085969 3089220 3093258 3098516 3101929 3104300 3107341 3111387 3114657 3115976 3119607 3123832 3124356 3124896 3125448 3128384
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution. US Nationwide and countries of AT, AU, BE, CA, CH, CL, CN, CZ, DB, DE, DK, EE, ES, FI, FR, GB, HK, IE, IL, IN, IT, JP, LT, LV, NL, NO, PL, PR, PT, RO, SE, SG, SI, TH, TR, and ZA.
  • Descripción del producto
    Smith & Nephew BEAVER Blade 4.0mm || Part Number: 72203307 || Orthopedic surgical instrument used in hip arthroscopy.
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew
Device Recall TOPAZ MicroDebrider
  • Modelo / Serial
    1031506, 1031507, 1032123, 1032325, 1032741, 1032742, 1033443, 1033965, 1033966, 1034397, 1039120, 1041765, 1044089, 1044090, 1045862, 1048237, 1048933, 1049185, 1052071, 1056212, 1060586, 1060979, 1063394, 1064599, 1067696, 1067748, 1069174, 1071358, 1074125, 1075714, 1070521, 1070812, 1071974, 1078025, 1077499, 1082811, 1084095, 1084094, 1085458, 1086436, 1086437, 1087917, 1094313, 1097573, 1103824, 1107183, 1107297, 1113562, 1113563, 1114534, 1114535, 1114536, 1115896, 1031518, 1032308, 1032309, 1032310, 1032755, 1032756, 1033972, 1033973, 1034225, 1034226, 1035283, 1035284, 1038547, 1043507, 1046556, 1047064, 1048722, 1049266, 1051812, 1052070, 1054443, 1055730, 1059865, 1063661, 1067691, 1067273, 1067747, 1068019, 1069172, 1071357, 1072853, 1072854, 1070497, 1070808, 1071971, 1076849, 1077450, 1079140, 1079220, 1078115, 1081753, 1082361, 1082810, 1086380, 1094312, 1094312, 1094721, 1097571, 1101041, 1107295, 1109045, 1111935, 1111936, 1113534, 1113535, 1113536, 1114532, 1115888, 1115891, 1116959, 1116130, 1116720, 1117209, 1117214, 1031341, 1032311, 1033761, 1034446, 1035691, 1035692, 1041775, 1043962, 1046557, 1048236, 1050067, 1052651, 1057008, 1058808, 1059867, 1063665, 1064594, 1067695, 1068021, 1071319, 1071320, 1073441, 1074876, 1077498, 1080520, 1114533, 1115893, 1031340, 1032962, 1033266, 1045359, 1047065, 1051331, 1056849, 1064592, 1067694, 1070709
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution-US (nationwide) and the following countries-Austria, Belgium, Bulgaria, Canada, Denmark, Estonia, Finland, France, Germany, Gibraltar, Great Britain, Greece, Ireland, Israel, Italy, Latvia, Netherlands, Norway, Poland, Portugal, Spain, Sweden, Switzerland, China, Hong Kong, India, Lebanon, Russia, Saudi Arabia, Singapore, South Africa, South Korea, Taiwan, Thailand, Turkey, United Arabic Emirates, Vietnam, Australia, Japan, New Zealand, Brazil, and Chile.
  • Descripción del producto
    TOPAZ MicroDebrider 0.8 mm REF AC4040-01; TOPAZ MicroDebrider IFS 0.8 mm REF ACH4040-01; TOPAZ MicroDebrider 0.8 mm REF Q6000-01; TOPAZ EPF MicroDebrider 0.8 mm 45 REF Q6002-01
  • Manufacturer
    ArthroCare Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall TOPAZ MicroDebrider
Device Recall Smith and Nephew TWINFIX QUICKT
  • Modelo / Serial
    Batch numbers: 50412843, 50477278, 50527184
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution. US nationwide, AT, AU, DE, FR, GB, JP, PT, and RU.
  • Descripción del producto
    Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter; Part Number: 7209417, for arthroscopic use.
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith and Nephew TWINFIX QUICKT
Device Recall RENASYS
  • Modelo / Serial
    Product Code 66020933 RENASYS G Small with Soft Port - Lots #'s 2015100134, 2015100313, 2015100314, 2016040686, and 2016040687 - US ONLY  Product Code 66020934 RENASYS G Medium with Soft Port - Lots #'s 2015100135, 2015100315, 2015100316, 2015110540, 2016040715, and 2016040963  US ONLY Product Code 66020935 RENASYS G Large with Soft Port- Lots #'s 2015100282, 2015100317, 2015110542, and 2016041021  US ONLY  Product Code 66020936 RENASYS G X Large with Soft Port Lot # 2016041035  US ONLY Product Code 66800394 RENASYS Transparent Film Lots #'s 2014010176, 2014011449, 2014030463, 2014040241, 2014050736, 2014051132, 2014061169, 2014113986, 2015020655, 2015040522, 2015050927, 015060209, 2015071095, 2015101044, 2015110749, 2015120664, and 2015121019 - GLOBAL Product Code 66800494 RENASYS G Medium Kit Flat Drain Lots #'s 02014P, 05014D, 06914E, 13414K, 15414T, 16014CV, 18114AV, 23214D, 25214J, and 26515H  GLOBAL (NOT US) Product Code 66800495 RENASYS G Large Kit 19Fr Round Drain Lots #'s 00815K, 14014L, 23314E, 25214H, and 32214D  GLOBAL (NOT US) Product Code 66800496 RENASYS G Large Kit Flat Drain Lots #'s 00815N, 01215G, 02214J, 05014F, 09014K, 09914K, 16014F, 17514T, 24114D, 25214K, 28015M, and 31714H  GLOBAL (NOT US) Product Code 66800497 REANSYS G X-Large Kit 19Fr Round Drain Lot # 05014M  GLOBAL (NOT US) Product Code 66800932 RENASYS High Output Fistula Kit Lots #'s 07715M, 09214H, 15514G, 18814K, and 27915G  GLOBAL (NOT US) Product Code 66800933 RENASYS G Small with Soft Port Lots #'s 2014010183, 2014011414, 2014020037, 2014021119, 2014021324, 2014021837, 2014030094, 2014030840, 2014030933, 2014031770, 2014040674, 2014041232, 2014041489, 2014050297, 2014050582, 2014051447, 2014051561, 2014060367, 2014060603, 2014060606, 2014071097, 2014080670, 2014080729, 2014091593, 2014091612, 2014091896, 2014091951, 2014102569, 2014103236, 2014103501, 2014103566, 2014125085, 2014125464, 2015016495, 2015016793, 2015016824, 2015020606, 2015020633, 2015021230, 015030904, 2015030938, 2015031168, 2015050397, 2015050706, 2015051210, 2015051333, 2015060715, 2015060718, 2015060878, 2015070001, 2015070021, 2015070057, 2015070243, 2015091343, 2015100464, 2015100652, 2015100707, 2015100859, 2015100968, 2015101007, 2015120041, 2015120046, 2015120052, 2015120061, 2015120411, 2016010750, 39907, 40151, 43250, 3251, and 43252  GLOBAL (NOT US) Product Code 66800934 RENASYS G Medium with Soft Port Lots #'s 2014010306, 2014010307, 2014010965, 2014011574, 2014020362, 2014020972, 2014021207, 2014021208, 2014021930, 2014021931, 2014022059, 2014022086, 2014030302, 2014030816, 2014030934, 2014031153, 2014031404, 2014031758, 2014040175, 2014041509, 2014041510, 2014042119, 2014050158, 2014050207, 2014050345, 2014050586, 201405062, 2014051041, 2014051041, 2014060684, 2014060833, 2014061007, 2014061442, 2014061669, 2014070114, 2014070520, 2014070979, 2014071068, 2014080794, 2014080836, 2014080909, 2014090181, 2014090267, 2014091758, 2014091835, 2014092091, 2014102295, 2014102318, 2014114098, 2014114125, 2014114183, 2014114284, 2014124756, 2014124797, 2014125114, 2014125177, 2014125233, 2015020672, 2015020750, 2015020781, 2015020841, 2015021100, 2015021102, 2015031154, 2015040916, 2015050291, 2015050995, 015050996, 2015051048, 2015051382, 2015051409, 2015060395, 2015060402, 2015060912, 2015060921, 2015060979, 2015061078, 2015070313, 2015070335, 2015070348, 2015091344, 2015100024, 2015100672, 2015101328, 2015101360, 2015101522, 2015110440, 2015110767, 2015110809, 2015110931, 2015110988, 2015110989, 2015111015, 2015111261, 2015121208, 2015121237, 2016010018, 2016010772, 2016010790, 39908, 40152, 43249, 43432, 43433, 43434, 43435, and 43558  GLOBAL (NOT US) Product Code 66800935 RENASYS G Large with Soft Port Lots #s 2014010875, 2014010876, 2014010919, 2014010940, 2014011209, 2014011229, 2014011418, 2014020026, 2014020946, 2014021122, 2014021838, 2014021839, 2014022085, 2014030813, 2014030841, 2014031293, 2014031354, 2014031399, 2014040860, 2014041269, 2014041410, 2014042109, 2014042113, 2014050898, 2014051040, 2014051655, 2014060089, 2014060169, 2014060274, 2014061051, 2014061333, 2014061438, 2014080369, 2014080549, 2014090036, 014091306, 2014102445, 2014102629, 2014102650, 2014114359, 2014114527, 2014114577, 2014124708, 2014125271, 2014125307, 2014125307, 2015020993, 2015021023, 2015040809, 2015051050, 2015051077, 2015060486, 2015060493, 2015060494, 2015060507, 015061065, 2015061135, 2015061224, 2015061265, 2015070371, 2015100539, 2015100585, 2015100603, 2015100611, 2015110023, 2015110257, 2015110291, 2015110435, 2015120445, 2015120457, 2015120752, 2015120762, 2016010895, 2016011075, 39909, 40153, 43535, 43559, 43565, and 43714  GLOBAL (NOT US) Product Code 66800936 RENASYS G X Large with Soft Port Lots #'s 2014010874, 2014010961, 2014040956, 2014050897, 2014080970, 2014103611, 2015021068, 2015021444, 2015040678, 2015070796, 2015100001, 2015100272, 2015101377, and 2015120027 -  GLOBAL (NOT US) Product Code 66801255 RENASYS G 10Fr Round Drain Kit Lots #'s 01415G, 02015E, 04916J, 16914G, 2014050828, 1015G, 21015H, and 32214L -  GLOBAL (NOT US) Product Code 66801256 RENASYS G 10mm Flat Drain Kit Lots #'s 05516D, 05715H, 08915E, 11214JV, 11414AV, 11414BV, 16914H, 2013050783, 2013060968, 20915T, 32115L, and 32314M  GLOBAL (NOT US) Product Code 66801257 RENASYS 15Fr Channel Drain Kit Lots #'s 08915D, 16914J, 19615V, 2014030237, 2014060209, 20815K, 20915G, 23014L, 28815K,32215G, and 32814J  GLOBAL (NOT US) Product Code 66801258 RENASYS G 19Fr Round Drain Kit Lots #'s 05316P, 17014K, 2014030238, 20915K, and 32314T  GLOBAL (NOT US)
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution to AK, AL, AR, AZ, CA, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TX, UT, VA, WA, WI, Hawaii, and Puerto Rico Argentina, Australia, Bermuda, Brazil, Brunai, Canada, Curacao, Germany, Great Britain, Hong Kong, Ireland, Jordan, Malaysia, New Zeland, Peru, Saudi Arabia, Serbia, Singapore, South Africa, SriLanka, Tunisia, Turkey, United Arab Emirates, and United Kingdom.
  • Descripción del producto
    RENASYS Sterile Transparent Film and all the RENASYS Dressing kits that contains the RENASYS Sterile Transparent Film || Is intended for patients who would benefit from a suction device (negative pressure) to help promote wound healing by removing fluids including irrigation and body fluids, wound exudates and infectious materials. Examples of appropriate wounds types include chronic, acute, traumatic, Sub-Acute and dehisced wounds, ulcers, (such as pressure and diabetic), partial thickness burns, flaps and grafts.
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall RENASYS
Device Recall RENASYS GO Negative Pressure Wound Therapy
  • Modelo / Serial
    Model No. 66800164; All pumps of this model are affected.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy, Rx only. || Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious materials. Used for chronic, acute, traumatic, subacute, and dehisced wounds/ulcers/partial thickness burns/flaps/grafts.
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall RENASYS GO Negative Pressure Wound Therapy
Device Recall RENASYS GO Negative Pressure Wound Therapy External Power Supply Unit
  • Modelo / Serial
    Model No. 66800161 when sold separately, Model No. 66800164 when sold with RENASYS GO NPWT Pump; Serial No. < than 144500875.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy External Power Supply Unit, Rx only. || Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious materials. Used for chronic, acute, traumatic, subacute, and dehisced wounds/ulcers/partial thickness burns/flaps/grafts.
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall RENASYS GO Negative Pressure Wound Therapy External Power Supply Unit
Device Recall Smith & Nephew Dyonics Saw Blade
  • Modelo / Serial
    Batch Numbers: 50586138 50458123 50418120 50339534 50306882 50285907 50248565 50231427 50197615 50171397 50158655 50138049 50119457 50089297 50082581 50069485
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela
  • Descripción del producto
    Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew Dyonics Saw Blade
Device Recall Smith & Nephew Dyonics Saw Blade
  • Modelo / Serial
    Batch Numbers: 50525150 50386077 50261802 50197616 50178740 50171398 50158656 50138050 50121538 50103379 50089298 50082582 50061131
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela
  • Descripción del producto
    Smith & Nephew Dyonics Saw Blade, Narrow, Product Number 3705
  • Manufacturer
    Smith & Nephew, Inc.
  • 4 Events
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew Dyonics Saw Blade
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew Dyonics Saw Blade
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew Dyonics Saw Blade
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew Dyonics Saw Blade
Device Recall Smith & Nephew Dyonics Saw Blade
  • Modelo / Serial
    Batch Numbers: 50439354 50393992 50252777 50208023 50171402 50138054 50103142 50066114 576304
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela
  • Descripción del producto
    Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew Dyonics Saw Blade
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM
  • Modelo / Serial
    Batch Numbers: G11243 G11244 G18810 G18813 G32171 G32172
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM || Product Number: 72204037 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM
  • Modelo / Serial
    Batch Numbers: G10766, G10782, G18814, G18815, G32178, G32179
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM || Product Number: 72204038 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM
  • Modelo / Serial
    Batch Numbers: G10785, G10787, G18816, G18817
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM || Product Number: 72204039 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM
  • Modelo / Serial
    Batch Numbers: F93290, F93297, G10709, G10712, G15944, G15945, G27849
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM || Product Number: 72204040 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM
  • Modelo / Serial
    Batch Numbers: F93305, F93306, G11233, G11234, G27843, G27847
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM || Product Number: 72204041 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM
  • Modelo / Serial
    Batch Numbers: F92143, F92147, G10380, G10382, G11216, G11217 G11231, G11232, G15940, G15943, G18835, G18836, G30219 G30220, G30254, G30255, G32180, G32182, G32183, G32184
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM || Product Number: 72204042 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM
  • Modelo / Serial
    Batch Numbers: F93301, F93303, G04665, G27840, G27841
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM || Product Number: 72204043 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM
  • Modelo / Serial
    Batch Numbers: F86213 ,F86216 , G04654, G04655, G04656, G10376 G10377, G11224, G11226, G11237, G11238, G15935, G15936, G15937, G18822, G18823, G18824, G18826, G18837, G18838, G18840, G18841, G30215, G30216, G30247, G30248, G30256, G32169, G32173, G32174 G32175, G32176, G32177
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM || Product Number: 72204044 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM
  • Modelo / Serial
    Batch Numbers: F93298, F93299, F93300,G11240 ,G11242, G30252, G30253
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM || Product Number: 72204045 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM
  • Modelo / Serial
    Batch Numbers: F91770, F92141, G10378, G10379, G10788, G10790 G11229, G11230, G11235, G11236, G15938, G15939, G18830, G18832 G27835, G27835, G27836, G30217, G30218, G30250, G30251, G32170
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM || Product Number: 72204046 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10.5MM
  • Modelo / Serial
    Batch Numbers: G10802 ,G10804, G18818
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE
  • Descripción del producto
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10.5MM || Product Number: 72204047 || The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
  • Manufacturer
    Smith & Nephew, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10.5MM
  • 1
  • 2
  • 3
  • …
  • Next ›
  • Last »

Acerca de la base de datos

Explore más de 120,000 registros de retiros, alertas y notificaciones de seguridad de dispositivos médicos y sus conexiones con los fabricantes.

  • Preguntas frecuentes
  • Acerca de la base de datos
  • Contáctenos
  • Créditos

Historias en su correo

¿Trabaja en la industria médica? ¿O tiene experiencia con algún dispositivo médico? Nuestra reportería no ha terminado. Queremos oír de usted.

¡Cuéntanos tu historia!

Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.

Descargar la data

La International Medical Devices Database está bajo la licencia Open Database License y sus contenidos bajo la licencia Creative Commons Attribution-ShareAlike . Al usar esta data, siempre citar al International Consortium of Investigative Journalists. Puede descargar acá una copia de la base de datos.

Descargar todo (zipped)