Hollister Ulc

Country not established FDA establishment FEI 3005028195

Devices: 0
Registrations: FDA
FDA recalls: 11 ongoing

No devices from this company are in the catalogue yet.

Company details

FDA FEI number: 3005028195
Address: FOXFORD RD., REHINS BALLINA Mayo

FDA recalls1

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

Recalls initiated per year

2017 0
2018 0
2019 0
2020 0
2021 0
2022 0
2023 0
2024 0
2025 0
2026 1

2026
- 14 Jul 2026 Z-2998-2026 Class II Ongoing Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might lead to genitourinary trauma or bleeding. Distribution: US Nationwide distribution. Submission number: K211436

This is an FDA establishment record without devices in deviCERTS.