French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by Medicina. The users concerned have received the attached mail (27/01/2015) (583 KB). This safety action is registered with the ANSM under the number 201500195. You will have the possibility of consulting its progress on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by Medicina. The users concerned received the attached mail (27/01/2015) (590 KB). This security action is registered with the ANSM under the number 201500201 .. You will have the possibility of consulting its progress report on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by Biomet Microfixation. The users concerned received the attached mail (17/02/2015) (180 KB). This safety action is registered with the ANSM under the number 201500205 .. You will have the possibility of consulting its progress status on the Directory of the reports of materielovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by Medicina. The users concerned received the attached mail (05/02/2015) (583 KB). This safety action is registered with the ANSM under n ° 201500233 .. You will have the possibility of consulting its progress report on the Directory of the reports of materiovigilance (05/02/2015) (583 ko) by entering this n ° registration.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
The ANSM has been informed of the implementation of a recall made by the company Zimmer .. The users concerned have received the attached mail (05/02/2015) (29 KB). Appendix 1 - List of concerned references (06/02/2015) (769 kb This safety action is registered with the ANSM under the n ° 201500407 .. You will be able to consult its progress report on the Directory of the reports of materialovigilanc by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by the company. The users concerned received the attached mail (19/02/2015) (18 KB). This safety action is registered with the ANSM under the number 201500429 .. You will have the possibility of consulting its progress report on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall by Euromi. The users concerned received the attached mail (11/02/2015) (497 KB). This security action is registered with the ANSM under the number 201500496 .. You will be able to consult its progress report on the Directory of the signaling of materiovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall by Clinical Innovations. The users concerned received the attached mail (05/02/2015) (133 KB). This security action is registered with the ANSM under the number 201500540 .. You will have the possibility of consulting its progress report on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
The ANSM has been informed of the implementation of a recall made by the company BIOMET .. The users concerned have received the attached mail. (04/02/2015) (4039 kb.) This security action is registered with the ANSM under the number 201500546 .. You will be able to consult its progress report on the Directory of the signaling of materialovigilanc by entering this n ° d 'recording.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by Mölnlycke Healthcare. The users concerned have received the attached mail (17/02/2015) (33 KB). This security action is registered with the ANSM under the number 201500743 .. You will have the possibility of consulting its progress report on the Directory of the reports of materielovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
The ANSM has been informed of the implementation of a recall made by the company STRYKER TRAUMA. The users concerned have received the attached mail. (10/02/2015) (52 KB) This safety action is registered with the ANSM under the number 201500859 .. You will be able to consult its progress report on the Directory of the reports of materovigilance (01/01/1970) (0 ko) by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
The ANSM has been informed of the implementation of a recall made by the company Amplitude. The users concerned have received the attached mail (06/02/2015) (91 KB). This safety action is registered with the ANSM under the number 201500963. You will have the possibility of consulting its progress report on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by Biomet. The users concerned received the attached mail (18/02/2015) (130 KB). This safety action is registered with the ANSM under the number 201501052 .. You will have the possibility of consulting its progress report on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by BBRAUN. The only user concerned in France received the attached mail (19/02/2015) (1003 KB). This security action is registered with the ANSM under the number 201501132. You will have the possibility of consulting its progress on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
The ANSM has been informed of the implementation of a recall made by ECOLAB / MICROTEK. The users and the distributors concerned have received the attached mail (04/02/2015) (207 KB). This safety action is registered with the ANSM under the number 201501209 .. You will be able to consult its progress on the Directory of the reports of materiovigilance. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
The ANSM has been informed of the implementation of a recall made by Smith & Nephew (Arthrocare). The users concerned received the attached mail (16/02/2015) (48 KB). This safety action is registered with the ANSM under the number 201501761. You will have the possibility of consulting its progress on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
The ANSM has been informed of the implementation of a withdrawal of product by the company EDWARDS LIFESCIENCES LLC .. The users concerned have received the attached mail (28/08/2015) (422 KB). This recall follows two previous security information, released in February and June 2015. This security action is registered with the ANSM under the number 201501845. You will be able to consult its progress on the Directory of materiovigilance reports by entering this number. Read too. Commander - Edwards Implementation System - Security Information of 25/02/201. Commander - Edwards Implementation System - Safety Information from 16/06/2015
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by CERAVER. The affected users have received the attached mail. (27/02/2015) (223 KB) This security action is registered with the ANSM under the number 201501897 .. You will be able to consult its progress report on the Directory of the reports of materialovigilanc by entering this n ° of 'recording.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by Terumo. The users concerned received the attached mail (19/03/2015) (99 KB). This safety action is registered with the ANSM under the number 201501986. You will have the possibility of consulting its progress on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by US Endoscopy. The affected users received the attached mail (16/03/2015) (52 KB). This safety action is registered with the ANSM under the number 201502721 .. You will have the possibility of consulting its progress report on the Directory of the reports of materielovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by STRYKER. The users concerned received the attached mail (24/04/2015) (72 KB). This safety action is registered with the ANSM under the number 201502126 .. You will have the possibility of consulting its progress report on the Directory of the reports of materialovigilanc. by entering this registration number .. Read more. Ancillary Material: Modular Blade Guide for Distal Femoral Resection Triathlon - Stryker - Safety Information (03/16/2015) (0 KB) (03/16/2015)
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by ARROW / TELEFLEX. The users concerned have received the attached mail (12/03/2015) (191 KB). This safety action is registered with the ANSM under the number 201502347. You will have the possibility of consulting its progress report on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by B BRAUN MEDICAL. The users concerned have received the attached mail (03/03/2015) (67 KB). This security action is registered with the ANSM under the number 201502428 .. You will have the possibility to consult its progress report on the Directory of the reports of materielovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by Medtronic. The 2 health facilities concerned in France received the following letter (19/03/2015) (103 KB). This safety action is registered with the ANSM under the number 201502509 .. You will have the possibility of consulting its progress report on the Directory of the reports of materialovigilanc. by entering this registration number.
French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Notas adicionales en la data
Acción
ANSM has been informed of the implementation of a recall made by MAQUET. The users concerned received the attached mail (26/03/2015) (324 KB). This safety action is registered with the ANSM under the number 201502617 .. You will be able to consult its progress report on the Directory of the reports of materielovigilanc. by entering this registration number.