#Defibtech reviver how to
#Defibtech reviver serial number
#Defibtech reviver software
#Defibtech reviver license

All affected AEDs operating with software version 2.004 or earlier are to remain in the field and in service throughout the field action process. The field action consists of a software change to the AED.

#Defibtech reviver serial number

If your DDU-100 series AED serial number DOES NOT fall within the listed range, your AED is not affected by this recall.Ī letter was also sent to the distributors and direct accounts that have received the affected product by first class mail with a prepaid, return written acknowledgement card. This information will expedite the process of upgrading your AEDs.' Note: 'it is very important for you to contact us either through the Defibtech website or return this card to confirm that you have received this notice.

Complete and return the confirmation form via fax to 1-20. The customers were instructed to do the following:ġ) Remove the pads from the storage pouch on the back of their DDU-100 series AED and inspect the 9-digit serial number label.Ģ)Carefully note the 9-digit serial number on the back of the AED, then visit the Defibtech website at and enter their serial number to determine if their AED is affected email their serial number and contact information to or call Defibtech directly at 1-87 or 1-20 and Defibtech will inform them if their unit is affected.ģ) If their AED is affected, confirm receipt of this notification with Defibtech as soon as possible by website and/or confirmation card. The letter describes the product, problem and actions to be taken. Vous pouvez télécharger une copie de la base de données ici.The firm, Defibtech, sent an 'URGENT MEDICAL DEVICE SAFETY INFORMATION AND CORRECTION' letter dated Mato its customers. Toujours citer le Consortium international des journalistes d'investigation lorsque ces données sont utilisées.

#Defibtech reviver license

La base de données internationale sur les dispositifs médicaux est sous licence Open Database License et ses contenus sous licence Creative Commons Attribution-ShareAlike. Ceux-ci doivent consulter leur médecin afin de déterminer si elle contient des informations pertinentes et si ces informations ont des implications médicales pour eux. Cette base de données n'a pas pour vocation de fournir des conseils aux patients. Le même implant peut avoir des noms différents selon les pays. Nous ne suggérons ou n'insinuons pas que des sociétés ou autres entités incluses dans la base de données internationale sur les dispositifs médicaux se livrent à un comportement illégal ou agissent de manière inappropriée. Les dispositifs médicaux contribuent à diagnostiquer, prévenir et traiter de nombreuses blessures et maladies. Vous travaillez dans le secteur médical? Vous avez vécu une expérience avec un dispositif médical? Notre projet n'est pas terminé.

#Defibtech reviver how to

Upon receipt of contact information from affected customers, Defibtech will send an upgrade kit to customers consisting of a software data card, instructions on how to perform the upgrade, and a pre-paid upgrade confirmation postcard that must be returned to Defibtech upon completionĮxplorez plus de 120,000 rappels, alertes et avis de sécurité concernant les dispositifs médicaux, ainsi que leurs liens avec leurs fabricants. The firm, Defibtech, sent an 'URGENT MEDICAL DEVICE SAFETY INFORMATION AND CORRECTION' letter dated Mato its customers.