FDA Device recall Z-2076-2025
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra by C R Bard, citing cather packaging may contain the incorrect French size.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2076-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-06-03 |
| Published | 2025-07-09 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | C R Bard |
| Distribution | US |
Product
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Reason
Cather packaging may contain the incorrect French size.
Identifiers
| code_info | Lot # NGJX2513/UDI: 00801741000294 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2076-2025%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.