• About the database
  • How to use the database
  • Download the data
  • FAQ
  • Credits
List view Cards view
  • Device 3726
  • Manufacturer 31827
  • Event 4366
  • Implant 434
Name Classification Manufacturer Risk Class Country Source
ILS Ethicon intraluminal stapler General and Plastic Surgery Devices manufacturer #121 Colombia INVIMA
Ethicon Hemorrhoidal Circular Staplers General and Plastic Surgery Devices manufacturer #121 Colombia INVIMA
Ethicon Proximate HCS Hemorrhoidal Circular Stapler and Accessories 33mm General and Plastic Surgery Devices Ethicon Endo-Surgery Inc New Zealand NZMMDSA
Ethicon Proximate PPH Hemorrhoidal Circulat Stapler and Accessories, 33mm General and Plastic Surgery Devices Ethicon Endo-Surgery Inc New Zealand NZMMDSA
tigerpaw system ii General and Plastic Surgery Devices LAAX Italy MSHM
Hemorrhoidal Circular Staplers Proximate-Ethicon Endo-Surgery General and Plastic Surgery Devices Ethicon France ANSM
Surgiflo MS0010 hemostatic matrix kits;Surgiflo hemostatic matrix kits with Thrombin MS0011 General and Plastic Surgery Devices Ethicon France ANSM
Bard Composix Kugel Wide Oval and Large Disk Wall Repair Implants General and Plastic Surgery Devices BARD France ANSM
Device Recall Firefly General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall Firefly General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall IS3000 da Vinci Si" Surgical System General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall JUPITER General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall CelluTome General and Plastic Surgery Devices KCI USA, INC. 1 United States USFDA
Device Recall Harmony vLED Surgical Lighting System General and Plastic Surgery Devices Steris Corporation 2 United States USFDA
Device Recall Malleable C Retractor General and Plastic Surgery Devices Synthes, Inc. 1 United States USFDA
Device Recall MENTOR MemoryGel Sizer General and Plastic Surgery Devices Mentor Texas, LP. Unclassified United States USFDA
Device Recall MAYFIELD Ultra 360 Base Unit General and Plastic Surgery Devices Integra LifeSciences Corporation 1 United States USFDA
Device Recall SurgiCounter Charging Cradle General and Plastic Surgery Devices Stryker Instruments Div. of Stryker Corporation 1 United States USFDA
Device Recall da Vinci Si Surgical System General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall Safety PICC Insertion Tray with Chloraprep OneStep General and Plastic Surgery Devices Custom Healthcare Systems, Inc. 1 United States USFDA
Device Recall da Vinci Harmonic ACE General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall da Vinci Harmonic ACE General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall StarBurst MRI SemiFlex Electrode Device General and Plastic Surgery Devices Angiodynamics 2 United States USFDA
Device Recall Intuitive Surgical EndoWrist Stabilizer Instrument General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall Synthes Recon Locking Aiming Arm for Lateral Entry Femoral NailsEX and the Thumb Screw for the Aim General and Plastic Surgery Devices Synthes, Inc. 1 United States USFDA
  • 1
  • 2
  • 3
  • …
  • Next ›
  • Last »

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

  • FAQ
  • About the database
  • Contact us
  • Credits

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.