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St Jude Medical Inc.: Medical Device Recalls in 2019

Updated on March 25, 2026.

According to to data from the FDA, there were 6 medical device recalls made by St Jude Medical Inc. in 2019. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2013
2014
2016
2017
2018
2019
  • ELLIPSE DR, REF: CD2377-36QC Implantable cardioverter defibrillators (ICDs)
  • ELLIPSE DR, Tiered-therapy cardioverter/defibrillator, REF: CD2411-36C, UDI: 05414734507585
  • ELLIPSE VR, Tiered-therapy cardioverter/defibrillator, REF: CD1411-36Q, UDI: 05414734507738
  • ELLIPSE DR, Tiered-therapy cardioverter/defibrillator, REF: CD2411-36Q, UDI: 05414734507615
  • ELLIPSE VR, REF: CD1377-36C Implantable cardioverter defibrillators (ICDs)
  • ELLIPSE VR, REF: CD1377-36QC Implantable cardioverter defibrillators (ICDs)
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