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  • Device 3026
  • Manufacturer 615
  • Event 124969
  • Implant 600
Name Date Date initiated Country Source
Recall of Device Recall Whatman Body Fluid Collection Paper 903 2009-05-06 United States USFDA
Recall of Device Recall Biomet BioloxDelta Modular Ceramic Head 2009-03-16 United States USFDA
Recall of Device Recall Biomet Modular TTPA Ceramic Head 2009-03-16 United States USFDA
Recall of Device Recall Boston Scientific Fort 2009-05-12 United States USFDA
Recall of Device Recall Boston Scientific, Fort 2009-05-12 United States USFDA
Recall of Device Recall Amico ECylinder Canister Holder 2009-05-19 United States USFDA
Recall of Device Recall Philips Easy Diagnost Eleva Conventional R/F system 2009-01-21 United States USFDA
Recall of Device Recall Body Fluid Collection Paper 2009-05-19 United States USFDA
Recall of Device Recall BD GeneOhm MRSA Assay 2008-11-11 United States USFDA
Recall of Device Recall Philips EasyVision MM workstation with software 2009-01-30 United States USFDA
Recall of Device Recall Instrument Manager software 2009-05-11 United States USFDA
Recall of Device Recall Remel Middlebrook 7H10 Agar 2009-05-06 United States USFDA
Recall of Device Recall Medtronic SIGMA 100/200/300 Series IPGs 2009-05-18 United States USFDA
Recall of Device Recall Medtronic KAPPA 600/700/900 Series Implantable Pulse Generators (IPGs) 2009-05-18 United States USFDA
Recall of Device Recall Medtronic SIGMA 100/200/300 Series IPGs 2009-05-18 United States USFDA
Recall of Device Recall Malibu Polyaxial Screw 2009-03-04 United States USFDA
Recall of NexGen 2006-10-10 United States USFDA
Recall of Device Recall OSS Letson Proximal Femoral Trial 7 cm 2009-05-19 United States USFDA
Recall of Device Recall OSS Elliptical Proximal Femoral Trial 7 cm 2009-05-19 United States USFDA
Recall of Device Recall OSS Elliptical Proximal Femoral Trial 7 cm 2009-05-19 United States USFDA
Recall of Device Recall Medtronic KAPPA 600/700/900 Series Implantable Pulse Generators (IPGs) 2009-05-18 United States USFDA
Recall of Device Recall Malibu Polyaxial Screw 2009-03-04 United States USFDA
Recall of Device Recall Malibu Polyaxial Screw 2009-03-04 United States USFDA
Recall of Device Recall Malibu Polyaxial Screw 2009-03-04 United States USFDA
Recall of Device Recall Malibu Polyaxial Screw 2009-03-04 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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