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  • Device 4199
  • Manufacturer 4199
  • Event 4307
  • Implant 0
Name Date Date initiated Country Source
Recall Or Safety Alert for Certain implants 2013-10-08 Spain AEMPSVFOI
Recall Or Safety Alert for Glenosphere and Base Plate of the Reverse Shoulder System Zimmer Trabecular Metal, 2014-03-12 Spain AEMPSVFOI
Recall Or Safety Alert for "Trabecular Metal Reverse Glenosphere Helmets", models 00-4309-071-36 and 00-4309-071-40, manufactured by Zimmer, Inc., USA. 2013-08-23 Spain AEMPSVFOI
Recall Or Safety Alert for shoulder, knee and hip implants 2016-02-19 Spain AEMPSVFOI
Recall Or Safety Alert for Trabecular Metal Knee and Hip Implants in Aluminum Bags 2016-06-22 Spain AEMPSVFOI
Recall Or Safety Alert for Guide needles, all lots labeled with an expiration date of 10 years. Distributed between August 2005 and December 2011. 2015-10-16 Spain AEMPSVFOI
Recall Or Safety Alert for Femoral impactor heads 2015-06-23 Spain AEMPSVFOI
Recall Or Safety Alert for 4.5 mm cortical screws, listed as compatible with the M / DN system (see Annex 1 with the complete list); all batches manufactured before December 2014 2015-06-12 Spain AEMPSVFOI
Recall Or Safety Alert for Brake Bracket Cemented Tibial Drill 15.7 + 30mm Person, 2015-06-09 Spain AEMPSVFOI
Recall Or Safety Alert for "Trilogy" bone screws of 6.5mm x 35mm and 6.5x25mm 2014-12-30 Spain AEMPSVFOI
Recall Or Safety Alert for Zimmer Person and Instrumental Knee System for Provisional Tibial Articular Surface (TASP) Zimmer Persona 2014-09-30 Spain AEMPSVFOI
Recall Or Safety Alert for Instrument trays of the anterior lumbar plate system (ALP) Trinica 2014-08-20 Spain AEMPSVFOI
Recall Or Safety Alert for Polyethylene implants Gender Solutions® Natural-Knee® Flex, Natural-Knee®, Natural-Knee® II, MOST OptionsTM and ApolloTM Systems 2014-04-23 Spain AEMPSVFOI
Recall Or Safety Alert for "Inserter Ardis" Model 96-701-10001, lots 61946711, 61946712, 61991588 and 62000412, manufactured between April 2012 and June 2012 and "TM ArdisTM intersomatic system 2013-02-12 Spain AEMPSVFOI
Recall Or Safety Alert for Versys provisional femoral heads, nos of catalog 00-7895-022,026,028,032,036,040-01 / 30 and slotted temporary femoral heads, nos of catalog 00-7803-022,026,028,032,036,040-01 / 14 2012-12-18 Spain AEMPSVFOI
Recall Or Safety Alert for "Proximal wedge of tibial articular surface Person" 2015-03-04 Spain AEMPSVFOI
Recall Or Safety Alert for Femoral heads and cones Biolox Delta Head, Durasul 2015-02-10 Spain AEMPSVFOI
Recall Or Safety Alert for Natural-Knee® patellar bearings 2014-10-07 Spain AEMPSVFOI
Recall Or Safety Alert for Certain lots of the Liner Impactor of Zimmer Trabecualr Metal Instrument for reverse shoulder. 2012-08-22 Spain AEMPSVFOI
Recall Or Safety Alert for "Zimmer Natural Nail CM Long" cephalometric nails, manufactured by Zimmer GmbH, Switzerland, between July 2009 and July 2015. 2015-10-20 Spain AEMPSVFOI
Recall Or Safety Alert for Revitan Stem System Review 2017-02-08 Spain AEMPSVFOI
Recall Or Safety Alert for System of titanium plates "Normed Fender Titan Plates 3.5 / 4.0". 2016-05-12 Spain AEMPSVFOI
Recall Or Safety Alert for Revitan system 2016-03-30 Spain AEMPSVFOI
Recall Or Safety Alert for Low profile cup Original ME Müller® 2016-01-12 Spain AEMPSVFOI
Recall Or Safety Alert for Orthopedic implants manufactured before March 2010. 2012-09-17 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.