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  • Device 26490
  • Manufacturer 33665
  • Event 35826
  • Implant 7175
Name Date Date initiated Country Source
Recall of Ophthalmic Valved Trocar Cannula (23G and 25G) 2015-08-11 United States USFDA
Recall of Fenestrated Bipolar Forceps 2015-08-08 United States USFDA
Recall of 8F Plastic Dignity MidSized CT Port 2012-04-12 United States USFDA
Recall of AutoPulse Resuscitation System 2012-08-08 United States USFDA
Recall of Brainlab Cranial Navigation System 2013-04-22 United States USFDA
Recall of HIVISION Preirus, Avius ultrasound systems 2011-04-18 United States USFDA
Recall of Regenerex Ringloc Acetabular Cup 2011-04-14 United States USFDA
Recall of Regenerex Ringloc Acetabular Cup 2011-04-14 United States USFDA
Recall of Regenerex Ringloc Acetabular Cup 2011-04-14 United States USFDA
Recall of Total Ossicular Replacement Prosthesis, CliP Piston MVP 2011-04-27 United States USFDA
Recall of Regenerex Ringloc Acetabular Cup 2011-04-14 United States USFDA
Recall of Regenerex Ringloc Acetabular Cup 2011-04-14 United States USFDA
Recall of Regenerex Ringloc Acetabular Cup 2011-04-14 United States USFDA
Recall of Regenerex Ringloc Acetabular Cup 2011-04-14 United States USFDA
Recall of Regenerex Ringloc Acetabular Cup 2011-04-14 United States USFDA
Recall of Regenerex Ringloc Acetabular Cup 2011-04-14 United States USFDA
Recall of Oxford Femoral Knee System 2011-04-22 United States USFDA
Recall of SCREENERS Dip Drug Test 2011-04-26 United States USFDA
Recall of ENDOFUSE(R) Fusion Rods 2011-04-20 United States USFDA
Recall of ENDOFUSE(R) Fusion Rods 2011-04-20 United States USFDA
Recall of B.Braun Celsite 2011-04-13 United States USFDA
Recall of SeraQuest CMV IgM United States USFDA
Recall of CDI 500 2011-04-21 United States USFDA
Recall of CDI 500 2011-04-21 United States USFDA
Recall of Harleco Giemsa Stain 2011-04-04 United States USFDA
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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.