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  • Dispositivo 26490
  • Fabricante 33665
  • Evento 35826
  • Implante 7175
Bard Orbiter PV Steerable Catheter || Item #: 320100 (Marketed in Europe Only)
  • Modelo / Serial
    All lot numbers were the 4th digit contains the letter A through M. Ex. 07A''A''1234
  • Distribución
    Nationwide
  • Descripción del producto
    Bard Orbiter PV Steerable Catheter || Item #: 320100 (Marketed in Europe Only)
  • Manufacturer
    C. R.Bard, Inc./Electrophysiology Division
  • 1 Event
    • Retiro De Equipo (Recall) de Bard Orbiter PV Steerable Catheter || Item #: 320100 (Marketed in Europe Only)
Device Recall Medtronic AVE
  • Modelo / Serial
    Lot Number: 122596
  • Clasificación del producto
    Cardiovascular Devices
  • Distribución
    AL, AR, KY, LA, MT, NH, NY, PA, WI Foreign: Japan, Hungary
  • Descripción del producto
    Z2 Guiding Catheter 6 F JR3.5 SH || Item No. : Z26JR35SH
  • Manufacturer
    Medtronic, Inc.
  • 2 Events
    • Retiro De Equipo (Recall) de Device Recall Medtronic AVE
    • Retiro De Equipo (Recall) de Device Recall Medtronic AVE
Stryker Advanced Cement Mixing System Bowl and 180 Gram Cement Cartridge with Break-Away Femoral ...
  • Modelo / Serial
    lot 03030232.
  • Clasificación del producto
    Orthopedic Devices
  • Distribución
    United States, Canada, Italy, Japan and United Kingdom
  • Descripción del producto
    Stryker Advanced Cement Mixing System Bowl and 180 Gram Cement Cartridge with Break-Away Femoral Nozzle for use with Stryker high vacuum cement injection system, 6 pack; part 0306-563-000.
  • Manufacturer
    Stryker Instruments, Instruments Div.
  • 1 Event
    • Retiro De Equipo (Recall) de Stryker Advanced Cement Mixing System Bowl and 180 Gram Cement Cartridge with Break-Away Femoral Nozzle for use with Stryker high vacuum cement injection system, 6 pack; part 0306-563-000.
Cook Polyvinyl Alcohol Foam (PVA ) Embolization Particles, particle size 47-90 microns, 1 cc; ord...
  • Modelo / Serial
    All units distributed from February 24, 2003 through June 26, 2003.
  • Distribución
    United States, Australia, Brazil, Canada, Denmark, Hong Kong, India, Israel, Japan and Taiwan.
  • Descripción del producto
    Cook Polyvinyl Alcohol Foam (PVA ) Embolization Particles, particle size 47-90 microns, 1 cc; order number PVA-50.
  • Manufacturer
    Cook, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Cook Polyvinyl Alcohol Foam (PVA ) Embolization Particles, particle size 47-90 microns, 1 cc; order number PVA-50.
Device Recall 9 French Super ArrowFlex Percutaneous Sheath Introducer Kit
  • Modelo / Serial
    Catalog numbers AK-07903-AG, SI-07903-AG, JM-07903-AG, and CI-07903-AG.
  • Clasificación del producto
    Cardiovascular Devices
  • Distribución
    The products were shipped to hospitals, distributors, dealers and sales representatives nationwide. The product was also shipped to export dealers in Finland, Australia, Italy, Brazil, Taiwan, New Zealand, Poland, United Kingdom, and Belgium and subsidiaries in Germany, France, Africa, Canada, Netherlands, SPain, and Greece.
  • Descripción del producto
    9 French Super Arrow-Flex Percutaneous Sheath Introducer Kit with Arrowg and Blue Antimicrobial Surface Sheath
  • Manufacturer
    Arrow International Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall 9 French Super ArrowFlex Percutaneous Sheath Introducer Kit
Device Recall Boston Scientific /Micorvasive
  • Modelo / Serial
    4097154 4126946 4145035 4158456 4193792 4212753 4221510 4231545 4256164 4262043 4258584 4282986 4313907 4323261 4349628 4375687 4392520 4405118 4408527 4414677 4425997 4464404 4464403 4468969 4494611 4528589 4537936 4550692 4557360 4562655 4579693 4583642 4625634 4628069 4639625 4652811 4689625 4701139 4701138 4727026 4742360 4764119 4764122 4774555   4788365 4823397 4830419 4845754 4900789 4910488 4915451 4935096 4963935 4963936 4983393 4992627 5007857 5019451 5022419 5038639 5065152 5121437 5129514 5140440 5155296 5158742 5169243 5173373 5182914 5186852 5205601 5223778 5227258 5238638 5246424 5251510 5269078 5288531 5301576 5320588 5371233 5427428 5440613 5473223 5501877 5505775 5511863 5547602
  • Distribución
    Nationwide
  • Descripción del producto
    ASAP Channel Cut Biopsy System, 15 gauge || Reference Number: 1390
  • Manufacturer
    Boston Scientific Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Boston Scientific /Micorvasive
Device Recall OmniDiagnost
  • Modelo / Serial
    OmniDiagnost User Interface PN 9896 000 59561, 9896 000 12381, 9896 000 58161;  The firm utilizes a ''site number'' specific to each unit: 101599, 103055, 103058, 100520, 100873, 101152, 101154, 101676, 101962, 102164, 102582, 102977, 103050, 103051, 103052, 103055, 103058, 103218, 103219, 104012, 104577, 104858, 104934, 105324, 105394, 13124, 38351, 50428, 76596, 76944, 76948, 82655, 83871, 83958, 84441, 84850, 85163, 85165, 86113, 86303, 86326, 86339, 86340, 86485, 86486, 86549, 86965, 86977, 87164, X1707, X1747, 104857
  • Clasificación del producto
    Radiology Devices
  • Distribución
    The firm distributed devices to 81 hospitals and medical centers located throughout the U.S.
  • Descripción del producto
    OmniDiagnost System
  • Manufacturer
    Philips Medical Systems Sales & Service Region No. America
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall OmniDiagnost
Amplicor [3] AV-HRP, Avidin-HRP (Horseradish Peroxidase) BGG Conjugate. || Kit: AMPLICOR M. avium...
  • Modelo / Serial
    Amplicor [3] AV-HRP, Lot No. E09569 found in kit lot:  Lot E12990, Material No. 20759880018, Exp. 11/2004.
  • Distribución
    ♦ Amplicor CT/NG CT Detection Kit, Lot No.E12231, Material No.20759392018, Expiration 2/2005 , Shipped To: Roche Diagnostics Corporation, 9115 Hague Road, P.O. Box 50457 Indianapolis, IN 46250-0457. ♦ Amplicor CT/NG NG Detection Kit, Lot No.E12647, Material No.20759406018, Expiration 2/2005, Shipped To: Roche Diagnostics Corporation, 9115 Hague Road, P.O. Box 50457 Indianapolis, IN 46250-0457. ♦ Amplicor HCV Detection Kit, v2.0, Lot No.F01023, Material No.21118439018, Expiration 5/2005, Shipped To: Roche Diagnostics Corporation, 9115 Hague Road, P.O. Box 50457 Indianapolis, IN 46250-0457. ♦ Amplicor IC Detection Kit, 96 tests, Lot No.E09554, Material No.20751952018, Expiration 5/2005, Shipped To: Roche Diagnostics Corporation, 9115 Hague Road, P.O. Box 50457 Indianapolis, IN 46250-0457. Export-U.S Distributed Products: AmpliCap HCV Monitor Test, Lot No.E09193, Material No.21111337018, Expiration 8/2004 , Shipped To: Roche Diagnostics KK, Nippon Roche KK, Kamakura Factory 200, Aza Sotokochi, Kajiwara, Kamakura City, Kanagawa Pref, Japan. Amplicor IC Detection Kit, Lot No.E13115, Material No.20763306122, Expiration 7/2005, Shipped To: Roche Diagnostics KK, Nippon Roche KK, Kamakura Factory 200, Aza Sotokochi, Kajiwara, Kamakura City, Kanagawa Pref, Japan; Shipped To: Roche Diagnostics Canada, 201 Boulevard Armand-Frappier, Laval QC H7V 4A2, Canada; Shipped To: Roche Diagnostics GmbH, GX-OSW, Sandhoferstr. 116, D-68305 Mannheim. Amplicor M. avium Detection Kit, Lot No.E12990, Material No.20759880018, Expiration 11/2004, Shipped To: Roche Diagnostics KK, Nippon Roche KK, Kamakura Factory 200, Aza Sotokochi, Kajiwara, Kamakura City, Kanagawa Pref, Japan. Amplicor MTB Detection Kit, Lot No.E13307, Material No.20757462122, Expiration 9/2004, Shipped To: Roche Diagnostics KK, Nippon Roche KK, Kamakura Factory 200, Aza Sotokochi, Kajiwara, Kamakura City, Kanagawa Pref, Japan; Shipped To: Roche Diagnostics Canada, 201 Boulevard Armand-Frappier, Laval QC H7V 4A2, Canada Shipped To: Roche Diagnostics GmbH, GX-OSW, Sandhoferstr. 116, D-68305 Mannheim. Amplicor NG Detection Kit, Lot No.E10894, Material No.20744026122, Expiration 2/2005, Shipped To: Roche Diagnostics KK, Nippon Roche KK, Kamakura Factory 200, Aza Sotokochi, Kajiwara, Kamakura City, Kanagawa Pref, Japan ; Shipped To: Roche Diagnostics Canada, 201 Boulevard Armand-Frappier, Laval QC H7V 4A2, Canada; Shipped To: Roche Diagnostics GmbH, GX-OSW, Sandhoferstr. 116, D-68305 Mannheim. There are no Govt. accounts.
  • Descripción del producto
    Amplicor [3] AV-HRP, Avidin-HRP (Horseradish Peroxidase) BGG Conjugate. || Kit: AMPLICOR M. avium Detection Kit, Export,RUO.
  • Manufacturer
    Roche Molecular Systems Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Amplicor [3] AV-HRP, Avidin-HRP (Horseradish Peroxidase) BGG Conjugate. || Kit: AMPLICOR M. avium Detection Kit, Export,RUO.
GSK
  • Modelo / Serial
    Shipper case lot #8008580, Retal Carton Lot #4543U8008580
  • Distribución
    US Nationwide
  • Descripción del producto
    Breathe Right Clear, 30 ct. carton., UPC 7-57145-00246-7 (US), UPC 9-300673-871749 (AU/NZ)
  • Manufacturer
    GSK Consumer Healthcare
  • 1 Event
    • Retiro De Equipo (Recall) de GSK
VITEK 2 AST P612
  • Modelo / Serial
    4920179103 24/May/18
  • Distribución
    Nationwide distribution in the U.S, including military and government sites. The product was also distributed to Algeria, Angola, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bosnia - Herzegovina, Brazil, Brunei, Bulgaria, Burkina Faso, Cambodia, Cameroun, Canada, Chad, Chile, China, Colombia, Congo, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republic, Dutch Antilles, Ecuador, Egypt, El Salvador, Estonia, Finland, France, Gabon, Gambia, Georgia, Germany, Greece, Grenada, Guatemala, Guinea, Haiti, Honduras, Hungary, India, Indonesia, Iraq, Israel, Italy, Ivory Coast, Japan, Jordan, Kazakhstan, Kenya, Uganda, Kuwait, Laos, Latvia, Lebanon, Lithuania, Malaysia, Mali, Malta, Mexico, Mongolia, Morocco, Mozambique, Myanmar, Netherlands, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Senegal, Serbia, Singapore, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sweden, Switzerland, Syria, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Venezuela, Vietnam, and Zimbabwe.
  • Descripción del producto
    VITEK¿ 2 Gram Positive Susceptibility card (AST-P612), REF 22359, 20 cards per carton.
  • Manufacturer
    Biomerieux Inc
  • 1 Event
    • Retiro De Equipo (Recall) de VITEK 2 AST P612
VITEK 2 AST N190
  • Modelo / Serial
    5600137203 12/Apr/18 5600171103 16/May/18 5600238103 22/Jul/18
  • Distribución
    Nationwide distribution in the U.S, including military and government sites. The product was also distributed to Algeria, Angola, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bosnia - Herzegovina, Brazil, Brunei, Bulgaria, Burkina Faso, Cambodia, Cameroun, Canada, Chad, Chile, China, Colombia, Congo, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republic, Dutch Antilles, Ecuador, Egypt, El Salvador, Estonia, Finland, France, Gabon, Gambia, Georgia, Germany, Greece, Grenada, Guatemala, Guinea, Haiti, Honduras, Hungary, India, Indonesia, Iraq, Israel, Italy, Ivory Coast, Japan, Jordan, Kazakhstan, Kenya, Uganda, Kuwait, Laos, Latvia, Lebanon, Lithuania, Malaysia, Mali, Malta, Mexico, Mongolia, Morocco, Mozambique, Myanmar, Netherlands, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Senegal, Serbia, Singapore, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sweden, Switzerland, Syria, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Venezuela, Vietnam, and Zimbabwe.
  • Descripción del producto
    VITEK¿ 2 Gram Negative Susceptibility card (AST-N190), REF 412548, 20 cards per carton.
  • Manufacturer
    Biomerieux Inc
  • 1 Event
    • Retiro De Equipo (Recall) de VITEK 2 AST N190
VITEK 2 AST N230
  • Modelo / Serial
    6300132203 07/Apr/18
  • Distribución
    Nationwide distribution in the U.S, including military and government sites. The product was also distributed to Algeria, Angola, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bosnia - Herzegovina, Brazil, Brunei, Bulgaria, Burkina Faso, Cambodia, Cameroun, Canada, Chad, Chile, China, Colombia, Congo, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republic, Dutch Antilles, Ecuador, Egypt, El Salvador, Estonia, Finland, France, Gabon, Gambia, Georgia, Germany, Greece, Grenada, Guatemala, Guinea, Haiti, Honduras, Hungary, India, Indonesia, Iraq, Israel, Italy, Ivory Coast, Japan, Jordan, Kazakhstan, Kenya, Uganda, Kuwait, Laos, Latvia, Lebanon, Lithuania, Malaysia, Mali, Malta, Mexico, Mongolia, Morocco, Mozambique, Myanmar, Netherlands, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Senegal, Serbia, Singapore, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sweden, Switzerland, Syria, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Venezuela, Vietnam, and Zimbabwe.
  • Descripción del producto
    VITEK¿ 2 Gram Negative Susceptibility card (AST-N230), REF 413147, 20 cards per carton.
  • Manufacturer
    Biomerieux Inc
  • 1 Event
    • Retiro De Equipo (Recall) de VITEK 2 AST N230
VITEK 2 AST P625
  • Modelo / Serial
    5350137203 12/Apr/18
  • Distribución
    Nationwide distribution in the U.S, including military and government sites. The product was also distributed to Algeria, Angola, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bosnia - Herzegovina, Brazil, Brunei, Bulgaria, Burkina Faso, Cambodia, Cameroun, Canada, Chad, Chile, China, Colombia, Congo, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republic, Dutch Antilles, Ecuador, Egypt, El Salvador, Estonia, Finland, France, Gabon, Gambia, Georgia, Germany, Greece, Grenada, Guatemala, Guinea, Haiti, Honduras, Hungary, India, Indonesia, Iraq, Israel, Italy, Ivory Coast, Japan, Jordan, Kazakhstan, Kenya, Uganda, Kuwait, Laos, Latvia, Lebanon, Lithuania, Malaysia, Mali, Malta, Mexico, Mongolia, Morocco, Mozambique, Myanmar, Netherlands, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Senegal, Serbia, Singapore, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sweden, Switzerland, Syria, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Venezuela, Vietnam, and Zimbabwe.
  • Descripción del producto
    VITEK¿ 2 Gram Negative Susceptibility card (AST-P625), REF 413727, 20 cards per carton.
  • Manufacturer
    Biomerieux Inc
  • 1 Event
    • Retiro De Equipo (Recall) de VITEK 2 AST P625
VITEK 2 AST N330
  • Modelo / Serial
    7700138203 13/Apr/18
  • Distribución
    Nationwide distribution in the U.S, including military and government sites. The product was also distributed to Algeria, Angola, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bosnia - Herzegovina, Brazil, Brunei, Bulgaria, Burkina Faso, Cambodia, Cameroun, Canada, Chad, Chile, China, Colombia, Congo, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republic, Dutch Antilles, Ecuador, Egypt, El Salvador, Estonia, Finland, France, Gabon, Gambia, Georgia, Germany, Greece, Grenada, Guatemala, Guinea, Haiti, Honduras, Hungary, India, Indonesia, Iraq, Israel, Italy, Ivory Coast, Japan, Jordan, Kazakhstan, Kenya, Uganda, Kuwait, Laos, Latvia, Lebanon, Lithuania, Malaysia, Mali, Malta, Mexico, Mongolia, Morocco, Mozambique, Myanmar, Netherlands, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Senegal, Serbia, Singapore, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sweden, Switzerland, Syria, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Venezuela, Vietnam, and Zimbabwe.
  • Descripción del producto
    VITEK¿ 2 Gram Negative Susceptibility card (AST-N330), IVD, REF 418674, 20 cards per carton.
  • Manufacturer
    Biomerieux Inc
  • 1 Event
    • Retiro De Equipo (Recall) de VITEK 2 AST N330
Coulter Clone B6-FITC Reagent
  • Modelo / Serial
    Lots 735512F, 735513F and 735514FR
  • Distribución
    Nationwide and to Canada
  • Descripción del producto
    Coulter Clone B6-FITC Reagent
  • Manufacturer
    Beckman Coulter Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Coulter Clone B6-FITC Reagent
Device Recall H. Pylori Ab Test CardSerum
  • Modelo / Serial
    Catalog number: 71046, All lots
  • Distribución
    Distributed in the states of CA, FL, NJ, TX, and NY.
  • Descripción del producto
    H. Pylori Ab Test Card-Serum; || LumiQuick, || Santa Clara, CA 95054
  • Manufacturer
    LumiQuick Diagnostics Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall H. Pylori Ab Test CardSerum
Device Recall Methamphetamine Strip
  • Modelo / Serial
    Catalog number: 74027, All lots
  • Distribución
    Distributed in the states of CA, FL, NJ, TX, and NY.
  • Descripción del producto
    Methamphetamine Strip; || LumiQuick, || Santa Clara, CA 95054
  • Manufacturer
    LumiQuick Diagnostics Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Methamphetamine Strip
Device Recall Propoxyphene Test Strip
  • Modelo / Serial
    Catalog number: 74051, All lots
  • Distribución
    Distributed in the states of CA, FL, NJ, TX, and NY.
  • Descripción del producto
    Propoxyphene Test Strip; || LumiQuick,. || Santa Clara, CA 95054
  • Manufacturer
    LumiQuick Diagnostics Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Propoxyphene Test Strip
Device Recall Troponin I test Card (Whole Blood)
  • Modelo / Serial
    Catalog number: 75002, All lots
  • Distribución
    Distributed in the states of CA, FL, NJ, TX, and NY.
  • Descripción del producto
    Troponin I test Card (Whole Blood); || LumiQuick,. || Santa Clara, CA 95054
  • Manufacturer
    LumiQuick Diagnostics Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Troponin I test Card (Whole Blood)
Device Recall Matrix MAX 3
  • Modelo / Serial
    Serial number 3337328
  • Distribución
    Worldwide Distribution-USA and Canada
  • Descripción del producto
    Matrix MAX3 Actuator, Catalog Number: MAX30 A300545A2510V000, SKF USA, Inc. Norristown, PA 19403
  • Manufacturer
    Skf USA Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Matrix MAX 3
Device Recall Matrix MAX 3
  • Modelo / Serial
    Serial number 3072047
  • Distribución
    Worldwide Distribution-USA and Canada
  • Descripción del producto
    Matrix MAX3 Actuator, Catalog Number: MAX30 A300515A254L000, SKF USA, Inc. Norristown, PA 19403
  • Manufacturer
    Skf USA Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Matrix MAX 3
Device Recall INTELECT ADVANCED
  • Modelo / Serial
    Serial numbers 1000 - 3993
  • Clasificación del producto
    Physical Medicine Devices
  • Distribución
    Worldwide Distribution - including USA
  • Descripción del producto
    INTELECT ADVANCED, Model No. 2762CC, Chattanooga Group, Hixson, TN 37343, Made in the USA, Not for sale in the U.S.A.
  • Manufacturer
    Chattanooga Corp Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall INTELECT ADVANCED
Device Recall Epic II VR Model V158
  • Modelo / Serial
    all serial codes
  • Distribución
    Nationwide and Internationally: Argentina, Australia, Austria, Barbados, Belgium, Bolivia, Brazil, Canada, Chile, China, Columbia, Costa Rica, Denmark, Dominican Republic, Ecuador, Finland, France, Germany, Hong Kong, Hungary, India, Italy, Japan, Korea, Malaysia,Mexico, Netherlands, New Zealand, Norway, Peru. Poland, Portugal, Republic of Panama, Singapore, Spain, Sweden, Switzerland, Taiwan, Thailand, Trinidad, United Kingdom, Uruguay and Venezuela.
  • Descripción del producto
    Implantable Cardioverter Defibrillator || EPIC II VR Tiered-therapy cardioverter/defibrillator, Model V-158
  • Manufacturer
    St Jude Medical CRMD
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Epic II VR Model V158
Synchron LX Clinical Systems, Operating Software, All versions.
  • Modelo / Serial
    All Versions.
  • Clasificación del producto
    Clinical Chemistry and Clinical Toxicology Devices
  • Descripción del producto
    Synchron LX Clinical Systems, Operating Software, All versions.
  • Manufacturer
    Beckman Coulter Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Synchron LX Clinical Systems, Operating Software, All versions.
Synthes Spiral Blade Component of the Synthes Modular Blade Plate System
  • Modelo / Serial
    All lots of Part Number: 02.122.555S, 55mm Spiral Blade, 14mm, Right-Sterile
  • Clasificación del producto
    Orthopedic Devices
  • Distribución
    Nationwide Distribution including AL, CA, GA, IA, IL, IN, MA, MI, MS, NC, NJ, NV, OH, PA, SC, SD, TN, and WV.
  • Descripción del producto
    02.122.555S, 55mm Spiral Blade, 14mm, Right-Sterile - Synthes Spiral Blade Component of the Synthes Modular Blade Plate System || For fixation of fractures and osteotomies of the proximal and distal femur in adolescents and adults.
  • Manufacturer
    Synthes USA (HQ), Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Synthes Spiral Blade Component of the Synthes Modular Blade Plate System
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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.