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  • Dispositivo 988
  • Fabricante 214
  • Evento 124969
  • Implante 233
Smith & Nephew
  • Modelo / Serial
    567531 50182767 50242031 50311086 50354626 50396028 50419909 50451050 50481583 586717 50193108 50251239 50311900 50361147 50400191 50423797 50451742 L50195027 50023445 50195027 50254749 50322127 50372399 50402518 50427083 50452777 50031093 50200477 50257710 50326789 50375128 50404802 50431408 50455222 50089906 50207485 50260093 50331945 50376693 50405482 50432856 50456255 50112893 50214248 50266143 50337081 50379780 50408076 50433676 50460255 50129647 50218992 50279513 50337265 50381258 50408437 50442599 50469461 50160551 50221872 50285674 50337464 50389830 50411651 50443725 50476967 50175558 50230673 50297948 50344790 50389832 50414388 50447281 50477073 50179006 50236269 50302624 50348085 50395177 50414909 50448747 50480681
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US Nationwide, Canada, Austria, Australia, Belgium, China, Spain, Finland, France, Great Britain, Greece, Germany, Hungary, India, Italy, Japan, Korea, Lithuania, Latvia, Netherlands, Poland, Portugal, Sweden, Thailand, Turkey, Ukraine and Venezuela
  • Descripción del producto
    Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm, Sterile || Part Number: 7209236 || Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects.
  • Manufacturer
    Smith & Nephew, Inc., Endoscopy Div.
  • 1 Event
    • Retiro De Equipo (Recall) de Smith & Nephew
Smith & Nephew
  • Modelo / Serial
    50069280 50214249 50260936 50334160 50380067 50410625 50442600 50084563 50217938 50266144 50337465 50383809 50412120 50448621 50097669 50227860 50276674 50352665 50385382 50415177 50451051 50112174 50231228 50282533 50353524 50389835 50416603 50451744 50117989 50236270 50310331 50356943 50391478 50424410 50452069 50131406 50242373 50317889 50362696 50396029 50428473 50455380 50139181 50246739 50320168 50370396 50399036 50428686 50457280 50148410 50254144 50324084 50372214 50401621 50432549 50461109 50199543 50254145 50328908 50374300 50404803 50436553 50469462 50203454 50258249 50332285 50378312 50407329 50436675 50475144 50481307
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US Nationwide, Canada, Austria, Australia, Belgium, China, Spain, Finland, France, Great Britain, Greece, Germany, Hungary, India, Italy, Japan, Korea, Lithuania, Latvia, Netherlands, Poland, Portugal, Sweden, Thailand, Turkey, Ukraine and Venezuela
  • Descripción del producto
    Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 8.5 mm, Sterile || Part Number: 7209237 || Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects.
  • Manufacturer
    Smith & Nephew, Inc., Endoscopy Div.
  • 1 Event
    • Retiro De Equipo (Recall) de Smith & Nephew
Smith and Nephew, Endo Femoral Aimer
  • Modelo / Serial
    Lot Number 50278012.
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- United States including Puerto Rico, Australia, Austria, Belgium, Canada, Costa Rica, Dubai, Finland, France, Germany, Great Britain, Netherlands, Norway, Portugal, Spain, Sweden, and Switzerland.
  • Descripción del producto
    AlMER ENDOFEMORAL 4MM OFFSET (PURPLE) || Part Number 72201714. || The product is an orthopedic device.
  • Manufacturer
    Smith & Nephew, Inc., Endoscopy Div.
  • 1 Event
    • Retiro De Equipo (Recall) de Smith and Nephew, Endo Femoral Aimer
Smith and Nephew, Endo Femoral Aimer
  • Modelo / Serial
    Lot Number 502780141
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- United States including Puerto Rico, Australia, Austria, Belgium, Canada, Costa Rica, Dubai, Finland, France, Germany, Great Britain, Netherlands, Norway, Portugal, Spain, Sweden, and Switzerland.
  • Descripción del producto
    AIMER ENDOFEMORAL 6MM OFFSET (GREEN) Part Number 72201716. || The product is an orthopedic device.
  • Manufacturer
    Smith & Nephew, Inc., Endoscopy Div.
  • 1 Event
    • Retiro De Equipo (Recall) de Smith and Nephew, Endo Femoral Aimer
Smith and Nephew, Endo Femoral Aimer
  • Modelo / Serial
    Lot Number 50278014.
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- United States including Puerto Rico, Australia, Austria, Belgium, Canada, Costa Rica, Dubai, Finland, France, Germany, Great Britain, Netherlands, Norway, Portugal, Spain, Sweden, and Switzerland.
  • Descripción del producto
    AIMER ENDOFEMORAL 6MM OFFSET (GREEN) Part Number 72201716. The product is an orthopedic device.
  • Manufacturer
    Smith & Nephew, Inc., Endoscopy Div.
  • 1 Event
    • Retiro De Equipo (Recall) de Smith and Nephew, Endo Femoral Aimer
TRIGEN SURESHOT Distal Targeting System
  • Modelo / Serial
    All serial numbers prior to and including ACA5
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA including AL, AR, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, MS, NC, NJ, NM, OH, PA, TN, TX, AND WA and the countries of Australia, Belgium, Canada, China, Denmark, Finland, France, Germany, Italy, Japan, Netherlands, Norway, South Africa, Spain, Sweden, Switzerland, Turkey, and the UK.
  • Descripción del producto
    smith & nephew TRIGEN SURESHOT Distal Targeting System, Trauma Interface, V2.0.2, Trauma Launcher V1.01.1 || Product is intended to be an intraoperative image-guided localization system. It is a computer-assisted orthopedic surgery tool to aid the surgeon with drill positioning for screws during intramedullary nail implantation.
  • Manufacturer
    Smith & Nephew Inc
  • 1 Event
    • Retiro De Equipo (Recall) de TRIGEN SURESHOT Distal Targeting System
Multiple Suture Anchors: Various models of HEALICOIL, TWINFIX, BIORAPTOR, FOOTPRINT Suture Anchor...
  • Modelo / Serial
    Multiple Suture Anchors: Various models of HEALICOIL, TWINFIX, BIORAPTOR, FOOTPRINT Suture Anchors (Used to attach the end of a synthetic or natural ligament to bone)Also Supplied separately and as part of the surgical arthroscopic procedure kit which is labelled with the suture model name.Multiple catalogue numbers affected All lot numbers affectedARTG Numbers: 109451 and 120338
  • Clasificación del producto
    Orthopedic Devices
  • Manufacturer
    Smith & Nephew Surgical Pty Ltd
  • 1 Event
    • Retiro De Equipo (Recall) de Multiple Suture Anchors: Various models of HEALICOIL, TWINFIX, BIORAPTOR, FOOTPRINT Suture Anchors (Used to attach the end of a synthetic or natural ligament to bone)Also Supplied separately and as part of the surgical arthroscopic procedure kit which is labelled with the suture model name.
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 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 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 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 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 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 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
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