FDA Device recall Z-2064-2018
Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
- FDA Device
- Class II
- terminated
- Published 2018-06-13
On 2018-06-13 the FDA classified a Class II recall of Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522) by C R Bard, citing foley Catheter with Incorrect Retainer Cap Print.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2064-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-12-13 |
| Published | 2018-06-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | C R Bard |
| Distribution | FL, MN, NY, TX |
Product
Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
Reason
Foley Catheter with Incorrect Retainer Cap Print
Identifiers
| code_info | Catalog # 01267522 Lot #'s: NGBR0383 and NGBR2129 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2064-2018%22
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