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  • Dispositivo 63
  • Fabricante 63
  • Evento 63
  • Implante 0
Alerta De Seguridad para Pluscan, Pluscan Alpha, Pluscan Alpha Safe, Plusflon, Plusflon Safe, Plu...
  • Tipo de evento
    Safety alert
  • Fecha
    2018-10-26
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2820543
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Voluntary recall of peripheral venous catheters from the Pluscan, Plusflon and Plusclip brands of the manufacturer Mediplus Limited (India)
Alerta De Seguridad para Provein Alpha and Provein Safe Alpha
  • Tipo de evento
    Safety alert
  • Fecha
    2018-10-26
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2820499
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Voluntary recall of peripheral venous catheters from Provein brand from manufacturer Lars Medicare Pvt. Ltd.
Alerta De Seguridad para Steam Pressure Sterilizer
  • Tipo de evento
    Safety alert
  • Fecha
    2018-10-22
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2817170
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Fake CE Certificate - Steam Pressure Sterilizer Manufacturer Wenzhou Longde Medical Technology Co., Ltd
Alerta De Seguridad para Wound dressings; Suture material; Staplers and clamps ; Dressing materia...
  • Tipo de evento
    Safety alert
  • Fecha
    2018-09-21
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2776248
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    False Certificates of Conformity - Manufacturer Paseca Healthcare LLP
Alerta De Seguridad para adbone®TCP crunch: 4-7 mm , batch number 02717 and reference TCP111120C
  • Tipo de evento
    Safety alert
  • Fecha
    2018-08-28
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2751453
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Counterfeit medical device - adbone®TCP crunch
Alerta De Seguridad para Patch Patches Hao Pi
  • Tipo de evento
    Safety alert
  • Fecha
    2018-08-28
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2751407
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Patch Patches Hao Pi from the manufacturer Dah Wei Biochemical Pharmaceutic International LTD
Alerta De Seguridad para JBP Nanoneedle Ultra Thin needle, JBP Nanocannula Thin walled 22G, JBP N...
  • Tipo de evento
    Safety alert
  • Fecha
    2018-08-10
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2742947
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Medical devices manufacturer Feel Tech Co., Ltd without valid CE conformity certificates
Alerta De Seguridad para unkown device
  • Tipo de evento
    Safety alert
  • Fecha
    2018-08-08
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2741270
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Condoms Durex Real Feel and Durex No Latex
Alerta De Seguridad para Timeless Skin Care Skin Roller
  • Tipo de evento
    Safety alert
  • Fecha
    2018-08-07
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2740568
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Timeless Skin Care Skin Roller
Alerta De Seguridad para Cardio M and Cardio M Plus 12-Lead Electrocardiographs
  • Tipo de evento
    Safety alert
  • Fecha
    2018-08-06
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2739190
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Cardio M and Cardio M Plus 12-Lead Electrocardiographs
Alerta De Seguridad para Philips HeartStart MRx External Automatic Defibrillators - M3535A and M3...
  • Tipo de evento
    Safety alert
  • Fecha
    2018-08-06
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2739010
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Philips HeartStart MRx External Automatic Defibrillators - M3535A and M3536A models
Alerta De Seguridad para Spengler Electronic Tensiometers
  • Tipo de evento
    Safety alert
  • Fecha
    2018-08-03
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2737509
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Spengler Electronic Tensiometers - change of user manual
Alerta De Seguridad para In vitro diagnostic device Prime Test Panel G
  • Tipo de evento
    Safety alert
  • Fecha
    2018-07-26
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2730505
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Non-compliance - In vitro diagnostic device Prime Test Panel G (Lithuania)
Alerta De Seguridad para Quick Diagnostic Manufacturer Tests
  • Tipo de evento
    Safety alert
  • Fecha
    2018-07-26
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2730459
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Non-Compliance Requirements - Quick Diagnostic Manufacturer Tests Assure Tech (Hangzhou) Co., Ltd (Lithuania)
Alerta De Seguridad para Balloon dilatation catheters, Balloon Expandable Stents, Self-Expandable...
  • Tipo de evento
    Safety alert
  • Fecha
    2018-07-16
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2720571
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    CE Certificate of False Compliance - Manufacturer Pan Medical US Corp. Ltd.
Alerta De Seguridad para Accu-Chek Aviva
  • Tipo de evento
    Safety alert
  • Fecha
    2018-05-29
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2655852
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Recall of batches of blood glucose strips Accu-Chek Aviva
Alerta De Seguridad para Magik Thread polydioxanone sutures
  • Tipo de evento
    Safety alert
  • Fecha
    2018-04-06
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2556588
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Magik Thread polydioxanone sutures from manufacturer Dermax Technology Limited
Alerta De Seguridad para Motus laser therapy
  • Tipo de evento
    Safety alert
  • Fecha
    2018-03-14
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2519220
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Motus laser therapy device from manufacturer Allroll Germany UG
Alerta De Seguridad para Sofiderm
  • Tipo de evento
    Safety alert
  • Fecha
    2018-03-14
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2519148
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Sofiderm device from manufacturer Hangzhou Techderm
Alerta De Seguridad para Oral hygiene sponge, oral sponge with aspiration, oral sponge with denti...
  • Tipo de evento
    Safety alert
  • Fecha
    2018-03-08
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2508995
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Manufacturer Changzou Reliance medical hygiene products Co.
Alerta De Seguridad para Viscoelastic solution - I-Visc
  • Tipo de evento
    Safety alert
  • Fecha
    2018-03-08
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2508644
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Viscoelastic solution - I-Visc
Alerta De Seguridad para Electrocoagulation probe for hemorrhoid treatment HPR45i
  • Tipo de evento
    Safety alert
  • Fecha
    2018-02-27
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2491784
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Electrocoagulation probe for hemorrhoid treatment HPR45i from manufacturer F-Care Systems NV
Alerta De Seguridad para Syringe pumps Alaris and Asena
  • Tipo de evento
    Safety alert
  • Fecha
    2018-02-19
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2474062
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Syringe pumps Alaris and Asena
Alerta De Seguridad para External lumbar and ventricular drainage systems Ceflui
  • Tipo de evento
    Safety alert
  • Fecha
    2018-02-09
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2458560
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    External lumbar and ventricular drainage systems Ceflui
Alerta De Seguridad para Semiconductor laser therapy device
  • Tipo de evento
    Safety alert
  • Fecha
    2018-01-18
  • País del evento
    Portugal
  • Fuente del evento
    NADHPIP
  • URL de la fuente del evento
    http://www.infarmed.pt/web/infarmed/alertas/-/journal_content/56/15786/2420622
  • Notas / Alertas
    Portuguese data is current through October 2018. All of the data comes from the National Authority of Drugs and Health Products (Infarmed, Portugal), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Portugal.
  • Notas adicionales en la data
  • Acción
    Semiconductor laser therapy device
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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.