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.
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 NOBEL BIOCARE AB. The users concerned received the attached mail (30/06/2015) (148 KB). This safety action is registered with the ANSM under the number 201508123 .. 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 the company BALT EXTRUSION. The only health facility concerned in France received the attached letter (03/07/2015) (103 KB). This safety action is registered with the ANSM under the number 201508124. 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 batch withdrawal carried out by BIOTRONIK AG. The users concerned received the attached mail (30/06/2015) (195 KB). This safety action is registered at ANSM under the number 201508170. 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 BIOSENSE WEBSTER INC. The affected users have received the attached mail (20/07/2015) (79 KB). This safety action is registered with the ANSM under the number 201508235. 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 carried out by the company BBRAUN MEDICAL .. The concerned users have received the attached mail (08/07/2015) (61 KB). This safety action is registered with the ANSM under the number 201508494. 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 carried out by the company NORTHERN DIGITAL INC .. The users concerned have received the attached mail (14/08/2015) (415 KB). This safety action is registered at ANSM under the number 201508591. 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
The ANSM has been informed of the implementation of a lot withdrawal carried out by MEDICINA Ltd. The users concerned received the attached mail (15/09/2015) (85 KB). This safety action is registered with the ANSM under the number 201508646. 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 carried out by the company DEPUY SYNTHES .. The users concerned have received the attached mail (08/07/2015) (60 KB). This safety action is registered with the ANSM under the number 201508679. 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 extension carried out by the company BIOMET. The users concerned have received the attached mail (30/07/2015) (194 KB). This safety action is registered with the ANSM under the number 201508720. You will be able to check its progress on the Directory of Materielovigilance Reports. by entering this registration number. Read too. AGC DUAL Articular 2000 femoral component (orthopedic surgery) - Biomet - Rappe. (2/13/2014)
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 NETWORK MEDICAL PRODUCTS LTD. The users concerned have received the attached mail (10/07/2015) (138 KB). This safety action is registered with the ANSM under the number 201508843 .. 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 batch recall extension carried out by BIOMET. The users concerned received the attached mail (30/07/2015) (212 KB). This safety action is registered with the ANSM under the number 201508867. 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
NB Advantage Beacon Tip, Royal Flush Plus Beacon Tip Angiography Catheters, Slip-Cath Beacon Tip Hydrophilic and Slip-Cath Shuttle Select. ANSM has been informed of the implementation of a complementary withdrawal of lots by COOK INCORPORATED. The users concerned have received the attached mail (04/11/2015) (138 KB) This security action is registered with the ANSM under the number 201509315. You will be able to consult its progress on the Directory of the reports. of materialovigilanc by entering this registration number Read also Previous batch recall issued on July 20th, 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
The ANSM has been informed of the implementation of a batch withdrawal carried out by COOK INCORPORATED. The users concerned received the attached mail (20/07/2015) (112 KB). This safety action is registered with the ANSM under the number 201509315. 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 products by the company COOK INCORPORATED .. The users concerned have received the attached mail (02/05/2016) (350 KB). This security action is registered with the ANSM under the number 201509315, and follows two previous security actions, in July 2015 and November 2015. Read more. Interventional Cardiology - Torcon NB Advantage Beacon Tip, Royal Flush Plus Beacon Tip and Slip-Cath Beacon Tip Angiography Catheters - Cook lncorporated (20/07/2015) - Recall of batches. Angiography Catheters (04/11/2015) - Cook lncorporated - Batch Recall
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 the company Research Instrument .. The users concerned have received the attached mail (18/05/2016) (329 ko). This safety action is registered at ANSM under the number 201604602.
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 MEDTRONIC. The users concerned have received the attached mail (22/07/2015) (154 KB). This safety action is registered with the ANSM under the number 201509564. 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.
Notas adicionales en la data
Acción
The ANSM has been informed of the implementation of a batch withdrawal carried out by SMITH & NEPHEW. The users concerned have received the attached letter (24/07/2015) (99 KB). This safety action is recorded at the ANSM under the number 201509565. 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 withdrawal made by the OTTOBOCK company. The users concerned have received the attached mail (24/07/2015) (41 KB). This security action is registered at ANSM under the number 201509764. 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 withdrawal made by the company OPTIMED. The users concerned have received the attached mail (30/07/2015) (215 KB). This security action is registered at ANSM under the number 201510010. 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 VYGON SA. The users concerned received the attached mail (07/08/2015) (552 KB). This security action is registered at ANSM under the number 201510027. You will be able to check its status on the Directory of Materiovigilance Reports by entering this registration number.