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 withdrawal of lots by the company BEAVER VISITEC INTERNATIONAL LIMITED .. The users concerned have received the attached mail (07/08/2015) (268 KB). This safety action is registered with the ANSM under the number 201506027. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 batch recall carried out by the company MEDISTOCK. The distributors concerned received the attached mail (20/05/2015) (421 KB). This safety action is registered with the ANSM under the number 201506038. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 batch recall carried out by BEAVER VISITEC INTERNATIONAL LIMITED. The users concerned received the attached mail (18/05/2015) (346 KB). This safety action is registered at ANSM under the number 201506049. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 batch withdrawal carried out by the company ORTHOFIX SRL .. The users concerned have received the attached mail. (11/06/2015) (2638 kb) This safety action is registered with the ANSM under the number 201506092. You will be able to consult its progress on the Directory of the signaling of materiovigilance 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
The ANSM has been informed of the implementation of a safety action carried out by PHILIPS. The users concerned received the attached mail (26/05/2015) (97 KB). This safety action is registered with the ANSM under the number 201506131. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 lot withdrawal carried out by MEDICREA INTERNATIONAL. The users concerned have received the attached mail (26/05/2015) (333 KB). This safety action is registered with the ANSM under the number 201506227. You will be able to consult its progress report on the Directory of the signaling 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 lot withdrawal carried out by BIOTRONIK AG. The users concerned received the attached mail (05/06/2015) (51 KB). This safety action is registered with the ANSM under the number 201506237. You will be able to consult 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 withdrawal of products by ZIMMER. The users concerned have received the attached mail (04/06/2015) (75 KB). This safety action is registered with the ANSM under the number 201506538. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 batch recall carried out by APPLIED DIABETES RESEARCH, INC. The concerned home health providers received the attached mail (22/06/2015) (98 KB). This safety action is registered with the ANSM under the number 201506662. You will be able to consult 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 lot withdrawal made by ZIMMER. The users concerned have received the attached mail (16/06/2015) (65 KB). This safety action is registered at ANSM under the number 201506714. You will be able to check its progress on the Directory of Materiovigilance Reports. 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 lot withdrawal carried out by BBRAUN MEDICAL. The affected users received the attached mail (05/06/2015) (113 KB). This safety action is registered with the ANSM under the number 201506804. You will be able to consult 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 lot withdrawal carried out by BIOMET FRANCE. The users concerned received the attached mail (01/06/2015) (133 KB). This safety action is registered with the ANSM under the number 201506843. You will be able to consult its progress report on the Directory of the signaling 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 lot withdrawal by the company Genzyme Europe BV The users concerned have received the attached mail (02/06/2015) (1229 ko). This safety action is registered with the ANSM under the number 201506904. 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 lot withdrawal carried out by ZIMMER INC. The users concerned have received the attached mail (10/06/2015) (90 KB). This safety action is registered with the ANSM under the number 201506916. You will be able to consult its status on the Directory of Materiovigilance Reports (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 batch withdrawal carried out by the company FH ORTHOPEDICS .. The users concerned have received the attached mail (09/06/2015) (191 KB). This safety action is registered with the ANSM under the number 201507063. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 lot withdrawal carried out by BBRAUN MELSUNGEN AG AESCULAP. The affected users have received the attached mail (08/06/2015) (91 KB). This safety action is registered with the ANSM under the number 201507266. You will be able to consult its progress report on the Directory of the signaling 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 products by the company BAUSCH AND LOMB INC .. The users concerned have received the attached mail (16/06/2015) (90 KB). This safety action is registered with the ANSM under the number 201507298. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 lot withdrawal carried out by DEPUY SYNTHES. The users concerned received the attached mail (15/06/2015) (58 KB). This safety action is registered with the ANSM under the number 201507363 .. 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
The ANSM has been informed of the implementation of a batch withdrawal made by the company STRYKER. The users concerned have received the attached mail (08/07/2015) (142 KB). This safety action is registered with ANSM under the number 201507594. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 withdrawal of products by ANIMAS CORPORATION. The concerned home health providers received the attached mail (26/06/2015) (229 KB). This safety action is registered with the ANSM under the number 201507697. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 attached mail is wrong. this message cancels and replaces the information posted on the morning of June 17, 2011. The ANSM has been informed of a withdrawal of lots made by the company MEDTRONIC .. The users concerned received the attached mail (17/06/2015) (35 KB). This safety action is registered at ANSM under the number 201507698. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 lot withdrawal carried out by MOLNLYCKE HEALTH CARE. The users concerned received the attached mail (22/06/2015) (84 KB). This safety action is registered with the ANSM under the number 201507831. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 product withdrawal action carried out by BOSTON SCIENTIFIC CORP. The users concerned received the attached mail (06/07/2015) (118 KB). This safety action is registered with the ANSM under the number 201507846. 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
The ANSM has been informed of the implementation of a batch recall carried out by IVOCLAR VIVADENT AG. The distributors and dentists concerned have received the attached letter (24/06/2015) (447 ko). This safety action is registered with the ANSM under the number 201507883. You will be able to check its progress on the Directory of Materielovigilance Reports. 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 made by the company ZIMMER SPINE .. The users concerned have received the attached mail (15/07/2015) (410 KB). This safety action is registered with the ANSM under the number 201507989. You will be able to check its progress on the Directory of Materielovigilance Reports. by entering this registration number.