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  • Device 6
  • Manufacturer 2
  • Event 124969
  • Implant 0
Name Date Date initiated Country Source
Recall of Device Recall Siemens Somatom CTs equipped with software syngo CT2010A, syngo CT2010B, syngo CT2011A and CT2012B 2012-11-27 United States USFDA
Recall of Device Recall ABX Micros IM2 2013-02-15 United States USFDA
Safety Alert for Peritoneal dialysis catheters Cuba HMC
Recall of Device Recall Philips MX 16Slice CT Scanner System 2012-12-19 United States USFDA
Recall of Device Recall Ingenuity TF PET/CT 2012-12-20 United States USFDA
Recall of Device Recall Endoscope Clip applier, Implantable Fastener and Accessories 2013-02-04 United States USFDA
Recall of Device Recall VITEK 2 60 computer system 2013-02-18 United States USFDA
Recall of Device Recall VITEK 2 XL computer system 2013-02-18 United States USFDA
Recall of Device Recall Asante Conset Infusion Set 2013-11-19 United States USFDA
Recall of Device Recall VITEK 2 Compact computer system 2013-02-18 United States USFDA
Recall of GE Healthcare Quasar Nuclear Medicine System, Hawkeye Option and Hawkeye 4 Option for Dual-Head Variable Angle Gamma Camera. Nuclear Medicine imaging systems. 2012-03-06 United States USFDA
Recall of Device Recall Synthes MultiVector Distractor, Multiaxial Mandible Distractor (Right), Part Number 487.966 2013-01-11 United States USFDA
Recall of Device Recall Synthes MultiVector Distractor Multiaxial Mandible Distractor (Left), Part Number 487.967 2013-01-11 United States USFDA
Recall of Device Recall Brilliance 6, 10, 16, 40, 64, Big Bore and the iCT, iCT SP, Ingenuity CT and MX8000 Dual v. EXP 2012-12-20 United States USFDA
Recall of Device Recall Ingenuity TF PET/CT 2013-01-21 United States USFDA
Recall of Device Recall Isolator Linear Pen, Electrosurgical cutting and coagulation device and accessories 2013-01-14 United States USFDA
Recall of Device Recall Aesculap(R) Bipolar Coagulator/Foot Pedal 2013-01-18 United States USFDA
Recall of Device Recall Medtronic DPL 2013-02-19 United States USFDA
Recall of Device Recall CO2 Incubators (General Purpose Incubator), 2012-11-29 United States USFDA
Recall of Device Recall Covidien Endo GIA 2013-02-11 United States USFDA
Recall of Device Recall AMSCO C and AMSCO 400 Steam Sterilizers 2013-02-12 United States USFDA
Recall of Device Recall Fixed Cervical Screws 2013-02-20 United States USFDA
Recall of Device Recall GOPump Elastomeric infusion PumpKit 2013-02-25 United States USFDA
Recall of Device Recall Zimmer Patient Helper Bed Frame Adapter Assembly 2013-02-14 United States USFDA
Recall of Device Recall Hickman and Leonard Catheters 2013-02-21 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.