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  • Device 26490
  • Manufacturer 33665
  • Event 35826
  • Implant 7175
Name Date Date initiated Country Source
Recall of Device Recall Doro Adapter 2007-02-14 United States USFDA
Recall of Device Recall Visitec 2007-03-02 United States USFDA
Recall of Device Recall Precision Xtra Blood Glucose monitoring system 2007-03-05 United States USFDA
Recall of Device Recall Gemini 16, GS, GXL, Precedence. 2006-11-06 United States USFDA
Recall of Device Recall Cook ATB Advance PTA Dilatation Catheter 2007-02-28 United States USFDA
Recall of Device Recall ARCHITECT STAT TroponinI Reagent 2007-03-08 United States USFDA
Recall of Device Recall Smith & Nephew Suture Passer 2007-03-01 United States USFDA
Recall of Device Recall Smith & Nephew 2007-03-01 United States USFDA
Recall of Device Recall Smith & Nephew 2007-03-01 United States USFDA
Recall of Device Recall AmpliChip CYP450 2007-03-09 United States USFDA
Recall of Device Recall AmpliChip CYP450 2007-03-09 United States USFDA
Recall of Device Recall Viatron CSeries dual chamber Rate Responsive Pacemakers 2007-02-05 United States USFDA
Recall of Device Recall Medfusion 3500 2007-02-03 United States USFDA
Recall of Device Recall Rusch MRI Conditional Fiber Optic Laryngoscope Kit 2007-03-01 United States USFDA
Recall of Device Recall Scanlan MobinUddin Vein Holder 2007-02-19 United States USFDA
Recall of Device Recall SeaClens Wound Cleanser 2007-02-14 United States USFDA
Recall of Device Recall Viatron TSeries Dual Chamber pacemakers 2007-02-05 United States USFDA
Recall of Device Recall BD 2007-02-15 United States USFDA
Recall of Device Recall COBAS Integra DIG 2007-03-16 United States USFDA
Recall of Device Recall Prostate Biopsy Needle 2007-01-19 United States USFDA
Recall of Device Recall Coaguchek 2007-02-28 United States USFDA
Recall of Device Recall LADAR6000 2007-02-21 United States USFDA
Recall of Device Recall DiaSorin TRYPSIK 2007-02-15 United States USFDA
Recall of Device Recall Puritan Bennett 840 Ventilator System 2007-03-12 United States USFDA
Recall of Device Recall AMS DURAII Distil Tips 2007-02-19 United States USFDA
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About this database

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

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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.

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