Class II — C.R. Bard, Inc.
| Recalling firm | C. R. Bard, Inc. |
|---|---|
| Registered facility | View this company's 19 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The device catheter tip was cut off (no tip) and the product packaging was not fully sealed. |
| Product | Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only. |
| Quantity | 9,800 Units |
| Distribution | Worldwide distribution - US Nationwide distribution and the countries of Australia, Canada. |
| Initiated | 2021-01-11 |
| Classified | 2021-04-16 |
| Terminated | 2023-02-02 |
| Recall number | Z-1431-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — C.R. Bard, Inc. (Z-1431-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/87163/
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