FDA Device recall Z-1431-2021
Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only
- FDA Device
- Class II
- terminated
- Published 2021-04-28
On 2021-04-28 the FDA classified a Class II recall of Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only by C R Bard, citing the device catheter tip was cut off (no tip) and the product packaging was not fully sealed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1431-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-01-11 |
| Published | 2021-04-28 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | C R Bard |
| Distribution | US |
Product
Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only.
Reason
The device catheter tip was cut off (no tip) and the product packaging was not fully sealed.
Identifiers
| code_info | Cat. No. 420712/Lot No. NGDY1813/ UDI (GTIN) (01)00801741038730(17)241130(10), Exp. Date 11/30/2024 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1431-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.