International safety notice

Desfibriladores automáticos implantables (DAI) y desfibriladores con terapia de resincronización cardiaca (TRC-D) Cobalt™ y Crome™. Ver modelos y números de serie afectados en la nota de aviso de la empresa.

Spain / AEMPS · ESP · Jul 12, 2022

Key facts

Title Desfibriladores automáticos implantables (DAI) y desfibriladores con terapia de resincronización cardiaca (TRC-D) Cobalt™ y Crome™. Ver modelos y números de serie afectados en la nota de aviso de la empresa.
Regulator Spain / AEMPS
Country ESP
Brand Desfibriladores automáticos implantables (DAI) y desfibriladores con terapia de resincronización cardiaca (TRC-D) Cobalt™ y Crome™. Ver modelos y números de serie afectados en la nota de aviso de la empresa.
Manufacturer Medtronic Inc, EEUU
Models RSG600480S, RSQ600871S, DTPA2D1, RSC601305S, RTC609040S, DVPB3D1, RTC600826S, RTC600990S, 2022-340, RTS601177S, DDPB3D4, RSQ601068S and 81 more
Event type Safety Notice
Date Jul 12, 2022

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices