Bard Clean-Cath Intermittent Catheter — Class II medical device recall Z-1431-2021
Terminated recall by C.R. Bard, Inc., reported 2021-04-28, distributed nationwide. The device catheter tip was cut off (no tip) and the product packaging was not fully sealed.
| Recall number | Z-1431-2021 |
|---|---|
| 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 | 2021-01-11 |
| Classified | 2021-04-16 |
| Reported by FDA | 2021-04-28 |
| Terminated | 2023-02-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA |
| Quantity | 9,800 units |
| UPC / GTIN / UDI-DI | 00801741038730 |
| Lot numbers | NGDY1813 |
| Model numbers | 420712 |
| Expiration dates | 2024-11-30 |
Product
Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only.
Reason for recall
The device catheter tip was cut off (no tip) and the product packaging was not fully sealed.
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-1431-2021. 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.