FDA Device recall Z-0666-2022
BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
- FDA Device
- Class II
- terminated
- Published 2022-03-02
On 2022-03-02 the FDA classified a Class II recall of BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C by C R Bard, citing there is a potential to leak from the catheter where it connects to the drain bag.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0666-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-01-27 |
| Published | 2022-03-02 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | C R Bard |
| Distribution | US |
Product
BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
Reason
There is a potential to leak from the catheter where it connects to the drain bag
Identifiers
| code_info | Serial Number/UDI NGEWX106/(01)00801741183232(17) NGEWX143/(01)00801741183232(17) NGFQ0368/(01)00801741183232(17) NGEW9106/(01)00801741183232(17) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Other recalls by C R Bard
- Products that contain the Pericare Wipes: *Bardex¿ I.C. Complete Care¿ Foley Catheter Tray REF: 300316A UDI codes: 00801741024344¿ 10801741…
FDA Device · Class II · 2026-09-16 · C R Bard - Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067¿ 108017411…
FDA Device · Class II · 2026-09-16 · C R Bard - Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314 947316 947318 UDI codes:…
FDA Device · Class II · 2026-09-16 · C R Bard - Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314AC UDI-DI code: 0…
FDA Device · Class II · 2026-09-16 · C R Bard - Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF: INTP16 INTS14 INTS14C INTS16 INTS16C PEDINTS06 PEDINTS08…
FDA Device · Class II · 2026-09-16 · C R Bard
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0666-2022%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.