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  • Device 788
  • Manufacturer 226
  • Event 124969
  • Implant 0
Name Classification Manufacturer Risk Class Country Source
Device Recall T3 (Trumpf Table Top) System Allen Medical Systems United States USFDA
Device Recall JUPITER General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall Steriseal BiManual Irrigating/Aspirating Handpiece Ophthalmic Devices Hill-Rom, Inc. 1 United States USFDA
Device Recall HillRom Liko General Hospital and Personal Use Devices Hill-Rom, Inc. 1 United States USFDA
Device Recall Jupiter, Mars, Titan, TruSystem and Saturn operating table systems General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall Power Bariatric Recliner General Hospital and Personal Use Devices Hill-Rom, Inc. 1 United States USFDA
Device Recall Liko Universal SlingBars General Hospital and Personal Use Devices Hill-Rom, Inc. 1 United States USFDA
Device Recall Mobile Column TruSystem 7500, Material Number 1717023; Mobile Column TruSystem 5500, Material Number General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall Stationary Column TruSystem 7599 General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall Floor Mounting Column TS 7500 U General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall Operating Table TruSystem 7000 U General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall Arthex S3 Arm Sleeve Connector Neurological Devices Allen Medical Systems, Inc. 1 United States USFDA
Device Recall Arthrex Shoulder Suspension Tower Neurological Devices Allen Medical Systems, Inc. 1 United States USFDA
Device Recall TruVidia Wireless Camera System General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
SlingBar 350 General Hospital and Personal Use Devices Hill-Rom, Inc. 1 United States USFDA
SlingBar 360 General Hospital and Personal Use Devices Hill-Rom, Inc. 1 United States USFDA
SlingBar 670 General Hospital and Personal Use Devices Hill-Rom, Inc. 1 United States USFDA
SlingBar Standard General Hospital and Personal Use Devices Hill-Rom, Inc. 1 United States USFDA
HillRom Likorall 200 General Hospital and Personal Use Devices Hill-Rom, Inc. 1 United States USFDA
Surgidyne SVac round fluted channel silicone drain General and Plastic Surgery Devices Aspen Surgical Products, Inc. 1 United States USFDA
Surgidyne SVac round fluted channel silicone drain kit General and Plastic Surgery Devices Aspen Surgical Products, Inc. 1 United States USFDA
Device Recall Titan General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall Titan General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall Titan General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 United States USFDA
Device Recall Titan General and Plastic Surgery Devices Trumpf Medical Systems, Inc. 1 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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