Skip to content

Penner Patient Care, INC

United Statesfrom the FDA registration address FDA establishment FEI 1922538

Devices
0
Registrations
FDA
FDA recalls
1010 ongoing

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
1922538
Address
101 Grant St, Aurora, NE, 68818

FDA recalls10

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

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 10
  • 2026 0

  • 2025

    • 13 Aug 2025 Z-1499-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772
    • 13 Aug 2025 Z-1500-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772
    • 13 Aug 2025 Z-1501-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772
    • 13 Aug 2025 Z-1502-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772
    • 13 Aug 2025 Z-1503-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772
    • 13 Aug 2025 Z-1504-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772
    • 13 Aug 2025 Z-1505-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772
    • 13 Aug 2025 Z-1506-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772
    • 13 Aug 2025 Z-1507-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772
    • 13 Aug 2025 Z-1508-2026 Class III Ongoing The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Submission number: K040772

This is an FDA establishment record without devices in deviCERTS.