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List view Cards view
  • Device 26490
  • Manufacturer 33665
  • Event 35826
  • Implant 7175
Name Classification Manufacturer Risk Class Country Source
Device Recall Natus neoBLUE 2 Phototherapy system General Hospital and Personal Use Devices Natus Medical Incorporated 2 United States USFDA
Device Recall ACCUCHEK Tender II Infusion Set General Hospital and Personal Use Devices Roche Diagnostics Operations, Inc. 2 United States USFDA
Device Recall ACCUCHEK Tender II Infusion Set General Hospital and Personal Use Devices Roche Diagnostics Operations, Inc. 2 United States USFDA
Device Recall ACCUCHEK Tender II Infusion Set General Hospital and Personal Use Devices Roche Diagnostics Operations, Inc. 2 United States USFDA
Device Recall ACCUCHEK Tender II Infusion Set General Hospital and Personal Use Devices Roche Diagnostics Operations, Inc. 2 United States USFDA
Device Recall ACCUCHEK Tender II Infusion Set General Hospital and Personal Use Devices Roche Diagnostics Operations, Inc. 2 United States USFDA
Device Recall Getinge 46Series Medical WasherDisinfector General Hospital and Personal Use Devices Getinge Disinfection Ab 2 United States USFDA
Device Recall SoftPath Clinical Chemistry and Clinical Toxicology Devices SCC Soft Computer 1 United States USFDA
Device Recall LUNA Chest, Model No. LU4006 Radiology Devices Novadaq Technologies, Inc. 2 United States USFDA
Device Recall LUNA Paq, Model No. LU3006 Radiology Devices Novadaq Technologies, Inc. 2 United States USFDA
Device Recall PKG, BIPOLAR FORCEPS, MICRO TIP Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BIPOLAR FORCEPS, FENESTRATED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BIPOLAR FORCEPS, PADDLE Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BIPOLAR FORCEPS, MICRO TIP Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BIPOLAR FORCEPS, FENESTRATED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, OPBIOPSY FORCEPS, SPOON JAW Stryker Endoscopy 2 United States USFDA
Device Recall PKG, FIXATION CLAMP 5MM WITH RATCHET Stryker Endoscopy 2 United States USFDA
Device Recall PKG, KNOT PUSHER 5MM OPEN Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MYOMA DRILL Stryker Endoscopy 2 United States USFDA
Device Recall PKG, PALPATION PROBE GRADUATED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, PORTIO ACORN SMALL ONLY Stryker Endoscopy 2 United States USFDA
Device Recall PKG, TROCAR 5.5MM PYRAMIDAL TIP Stryker Endoscopy 2 United States USFDA
Device Recall PKG, OBTURATOR, 5.5MM FOR HASSON CANNULA Stryker Endoscopy 2 United States USFDA
Device Recall PKG, CANNULA 5.5MM AUTOMATIC VALVE STOP COCK W/O TROCAR Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MARYLAND FORCEPS, CURVED Stryker Endoscopy 2 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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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.