FDA Device recall Z-2532-2021
Catalog A800365, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
- FDA Device
- Class II
- ongoing
- Published 2021-09-29
On 2021-09-29 the FDA classified a Class II recall of Catalog A800365, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray by C R Bard, citing there is potential for packaging defects that may impact the sterile barrier.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2532-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-08-05 |
| Published | 2021-09-29 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | C R Bard |
| Distribution | US |
Product
Catalog A800365, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
Reason
There is potential for packaging defects that may impact the sterile barrier.
Identifiers
| code_info | Catalog A800365, Lots: NGFR3131, UDI (01)00801741073960(17)201220(10); NGFR3295, UDI (01)00801741073960(17)201220(10);…Catalog A800365, Lots: NGFR3131, UDI (01)00801741073960(17)201220(10); NGFR3295, UDI (01)00801741073960(17)201220(10); NGFR4413, UDI (01)00801741073960(17)201220(10); NGFR4599, UDI (01)00801741073960(17)201220(10); and NGFS3150 UDI (01)00801741073960(17)201220(10) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2532-2021%22
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