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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a batch removal action carried out by DEDIENNE SANTE. The users concerned have received the attached mail (01/10/2015) (113 KB). This safety action is registered with the ANSM under the number 201512607. You will be able to consult its progress status on the Directory of Materielovigilanc 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a lot withdrawal action carried out by AMPLITUDE. The users concerned have received the attached mail (29/09/2015) (204 KB). This safety action is registered with the ANSM under the number 201512661. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a withdrawal of product by the company KISCO INTERNATIONAL. The users concerned have received the attached mail (07/10/2015) (1557 KB). This safety action is registered with the ANSM under the number 201512699. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a device recall carried out by MEDTRONIC INC. The concerned home health providers received the attached mail (07/10/2015) (271 ko). This safety action is registered with the ANSM under the number 201512745. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a withdrawal of product made by the company ETHICON. The users concerned have received the attached mail (15/10/2015) (253 KB). This safety action is registered with the ANSM under the number 201513015. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of the lot withdrawal carried out by INSULET CORPORATION. The affected users received the attached mail (07/01/2016) (374 KB). This safety action is registered with the ANSM under the number 201513045. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a batch withdrawal carried out by the company LABORATOIRES URGO. The affected users have received the attached mail (09/10/2015) (144 KB). This safety action is registered with the ANSM under the number 201513182. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a lot withdrawal by UPSA SAS. The users concerned received the attached mail (30/10/2015) (492 KB). This safety action is registered with ANSM under the number 201513364. 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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a batch withdrawal action carried out by STRYKER. The users concerned have received the attached mail (13/11/2015) (201 KB). This safety action is registered with the ANSM under the number 201513378. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a batch withdrawal action carried out by MEDICREA. The users concerned received the attached mail (19/10/2015) (52 KB). This safety action is registered with the ANSM under the number 201513409. You will be able to consult its progress on the Directory of the signaling of materiovigilance (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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a withdrawal of product made by the company BIOMET 3i .. The users concerned have received the attached mail (27/10/2015) (23 KB). This security action is registered at ANSM under the number 201513510. 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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a lot withdrawal action carried out by INTEGRA LIFESCIENCES. The users concerned have received the attached letter (26/10/2015) (487 KB). This safety action is registered with ANSM under the number 201513512. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a batch withdrawal carried out by VBM MEDIZINTECHNIK GMBH and implemented in France by MEDTRONIC / COVIDIEN. The users concerned have received the attached mail (26/10/2015) (451 KB). This security action is registered at ANSM under the number 201513617. 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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a lot withdrawal carried out by BEAVER VISITEC INTERNATIONAL LIMITED. The users concerned have received the attached letter (27/10/2015) (260 KB). This safety action is registered at ANSM under the number 201513629. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a lot withdrawal carried out by B. BRAUN AVITUM FRANCE. The users concerned have received the attached mail (23/10/2015) (36 KB). This safety action is registered with the ANSM under the number 201513785. 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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a lot withdrawal carried out by the company THUASNE. The users concerned have received the attached mail (30/10/2015) (147 KB). This security action is registered at ANSM under the number 201513993. 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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a lot withdrawal carried out by MEDTRONIC. The users concerned have received the attached letter. (03/11/2015) (328 KB) This security action is registered with the ANSM under the number 201514030. You will be able to consult its progress on the Directory of the signaling 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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a withdrawal of lots made by the company Medtronic / Covidien .. The user site concerned received the attached mail (05/11/2015) (180 KB). This security action is registered with ANSM under the number 201514133. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a withdrawal of lots by ARROW INTERNATIONAL. The users concerned have received the attached mail (01/12/2015) (197 KB). This safety action is registered with the ANSM under the number 201514145. 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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a batch withdrawal made by Novatech SA. The users concerned have received the attached letter (03/11/2015) (264 KB). This security action is recorded at ANSM under the number 201514149. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a product withdrawal carried out by MEDICO SPA. The 2 establishments concerned received the attached mail (19/11/2015) (394 ko). Further investigations by the ANSM are in progress. This safety action is registered with the ANSM under the number 201514268. You will be able to consult its progress on the Directory of the reports of materialovigilanc. by entering this registration number. Read auss. Heart stimulation probe - MG Phymos 4 R Lead, Medico SPA - Medico SPA - Safety Information. (5/13/2016)
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.
Notes supplémentaires dans les données
Action
The ANSM has been informed of the implementation of a safety action and a withdrawal of product carried out by ST JUDE MEDICAL INC. The 2 health establishments concerned in France have received the attached mail (13/11/2015) (111 ko). Further investigations by the ANSM are in progress. This safety action is registered with the ANSM under the number 201514404. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a batch withdrawal carried out by COOK. The affected users have received the attached mail (05/11/2015) (113 KB). This safety action is registered with the ANSM under the number 201514440. You will be able to consult its progress 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a lot withdrawal carried out by LEMAITRE VASCULAR INC. The users concerned received the attached mail (16/11/2015) (557 KB). This security action is registered with the ANSM under the number 201514478. 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.
Notes supplémentaires dans les données
Action
ANSM has been informed of the implementation of a lot withdrawal carried out by AESCULAP AG. The affected users have received the attached mail (10/11/2015) (48 KB). This safety action is registered with the ANSM under the number 201514496. You will be able to consult its progress on the Directory of the reports of materialovigilanc. by entering this registration number.