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  • Device 6
  • Manufacturer 2
  • Event 124969
  • Implant 0
Name Date Date initiated Country Source
Recall Or Safety Alert for Fabian HFO respirators, models 7200, 7200.i, 7201, and Fabian evolution, models 7250, 7250.N 2016-11-28 Spain AEMPSVFOI
Recall Or Safety Alert for Standing Vacuum Pump, reference 271 000 701, lot 10707-1 2016-05-04 Spain AEMPSVFOI
Recall Or Safety Alert for Urinary test ImmuView® S. pneumoniae and L. pneumophila. 2017-04-10 Spain AEMPSVFOI
Recall Or Safety Alert for AeriSeal® system, reference numbers 30300 and 30304, AeriSeal® accessory kit reference number 30100 and AeriSeal® accessories 2013-05-08 Spain AEMPSVFOI
Recall Or Safety Alert for "Camilla MRI, non-magnetic", model 7437549, serial numbers prior to 2010613130802001.001 2014-03-24 Spain AEMPSVFOI
Recall Or Safety Alert for Digital detectors for size 35 * 45 cm DX-D 10G, DX-D 10C, DX-D 20G and DX-D 20C 2012-04-09 Spain AEMPSVFOI
Recall Or Safety Alert for IMPAX 6.4 (versions prior to 6.4 su09) integrated with Agfa RIS (QDOC) 2012-08-08 Spain AEMPSVFOI
Recall Or Safety Alert for IMPAX RIS software 5.8 and higher 2014-03-06 Spain AEMPSVFOI
Recall Or Safety Alert for NX 3.0.8950 image processing software from the NX workstation 2017-01-20 Spain AEMPSVFOI
Recall Or Safety Alert for Drystar DT2 MAMMO films, ref: ERE5C and ERE6E, lot 36130026 and cutting plane AM940 2012-04-16 Spain AEMPSVFOI
Recall Or Safety Alert for IMPAX 5.2 DB Server 2013-10-18 Spain AEMPSVFOI
Recall Or Safety Alert for Mobile X-ray digital radiography system DX-D 100 2016-02-17 Spain AEMPSVFOI
Recall Or Safety Alert for Direct X-ray system DX-D 600 2016-05-18 Spain AEMPSVFOI
Recall Or Safety Alert for Dako Omnis, model GI100, software versions TRD 1.3 and TRD 1.4 2015-06-24 Spain AEMPSVFOI
Recall Or Safety Alert for Kit HER2 CISH pharmDx, code SK109, lot 20031665. 2016-06-24 Spain AEMPSVFOI
Recall Or Safety Alert for Automated system for the immunohistochemical diagnosis Autostainer Link 48 (AS480), with version 4.0 of the DakolinkTM software 2014-10-10 Spain AEMPSVFOI
Recall Or Safety Alert for Centrifuge "Rotofix 32A", serial numbers: 15049, 15058, 15449, 15454, 15538 and 15539, manufactured by Andreas Hettich GmbH Co.KG., Germany 2013-04-19 Spain AEMPSVFOI
Recall Or Safety Alert for Mini Fly patient cranes, reference AD915 2016-02-29 Spain AEMPSVFOI
Recall Or Safety Alert for Strattice ™ Tissue Reconstruction Matrix 2015-08-14 Spain AEMPSVFOI
Recall Or Safety Alert for Arsenal nut, reference 47127, subcomponent of the Arsenal spinal fixation system 2016-10-14 Spain AEMPSVFOI
Recall Or Safety Alert for Ambula® AuraGain ™ single-use laryngeal mask 2015-12-22 Spain AEMPSVFOI
Recall Or Safety Alert for "Needle pins" included in the "AdVance® XP male band systems" 2014-08-07 Spain AEMPSVFOI
Recall Or Safety Alert for "Needle pins" included in the "AdVance® XP male band system", reference 720163-01, supplied as of August 1, 2014 with expiration date of 1 year. 2014-11-11 Spain AEMPSVFOI
Recall Or Safety Alert for "Reusable orthopedic surgical instruments" 2014-12-15 Spain AEMPSVFOI
Recall Or Safety Alert for PICC BioFlo catheters with PASV and ENDEXO valve technology 2016-04-27 Spain AEMPSVFOI
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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.