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Sorin CRM SAS

Country not established FDA establishment FEI 3008159616

Devices
0
Registrations
FDA
FDA recalls
2

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3008159616
Address
4, avenue Reaumur, CLAMART Hauts-de-Seine

FDA recalls2

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

Recalls initiated per year

  • 2017 0
  • 2018 2
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 0

  • 2018

    • 9 Jul 2018 Z-2824-2018 Class II Terminated Hardware configuration may lead to overconsumption, followed by loss of pacing and sensing capabilities. The device then cannot identify an arrhythmia that would require defibrillation shock therapy. Distribution: US distribution to: NJ, AZ, MS, OK, LA, PA, FL, MI, IL, and MS Submission number: P060027S079
    • 9 Jul 2018 Z-2825-2018 Class II Terminated Hardware configuration may lead to overconsumption, followed by loss of pacing and sensing capabilities. The device then cannot identify an arrhythmia that would require defibrillation shock therapy. Distribution: US distribution to: NJ, AZ, MS, OK, LA, PA, FL, MI, IL, and MS Submission number: P060027S079

This is an FDA establishment record without devices in deviCERTS.