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Ebi Patient Care, Inc.

Country not established FDA establishment FEI 3003435252

Devices
0
Registrations
FDA
FDA recalls
2

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3003435252
Address
484 Calle E, GUAYNABO, PR, 00969

FDA recalls2

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

Recalls initiated per year

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

  • 2017

    • 20 Apr 2017 Z-2118-2017 Class I Terminated Zimmer Biomet is conducting a medical device field action for the SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulator products due to higher than allowed cytotoxicity levels found during routine process monitoring with the product. Distribution: Nationwide distribution only. Submission numbers: P850035, P850035S031
    • 20 Apr 2017 Z-2119-2017 Class I Terminated Zimmer Biomet is conducting a medical device field action for the SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulator products due to higher than allowed cytotoxicity levels found during routine process monitoring with the product. Distribution: Nationwide distribution only. Submission number: P850035

This is an FDA establishment record without devices in deviCERTS.