Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter — Class II medical device recall Z-2064-2018
Terminated recall by C.R. Bard, Inc., reported 2018-06-13, distributed in FL, MN, NY, TX. Foley Catheter with Incorrect Retainer Cap Print
| Recall number | Z-2064-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | C.R. Bard, Inc., Covington, GA, United States |
| Recall initiated | 2017-12-13 |
| Classified | 2018-06-06 |
| Reported by FDA | 2018-06-13 |
| Terminated | 2020-12-14 |
| Distributed | FL, MN, NY, TX |
| Countries outside the US | CA, JP, TW |
| Lot numbers | NGBR0383, NGBR2129 |
| Model numbers | 01267522 |
Product
Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
Reason for recall
Foley Catheter with Incorrect Retainer Cap Print
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2064-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.