FDA Device recall Z-0790-2024
Bard Nasogastric Sump Tube with ENFit, 10Fr., 36in Long, REF EN0042100
- FDA Device
- Class II
- ongoing
- Published 2024-01-31
On 2024-01-31 the FDA classified a Class II recall of Bard Nasogastric Sump Tube with ENFit, 10Fr., 36in Long, REF EN0042100 by C R Bard, citing BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage oc….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0790-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-12-20 |
| Published | 2024-01-31 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | C R Bard |
| Distribution | n/a |
Product
Bard Nasogastric Sump Tube with ENFit, 10Fr., 36in Long, REF EN0042100
Reason
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
Identifiers
| code_info | UDI/DI 00801741113772, Lot/Serial Numbers: NGEQ3034, NGER3656, NGFX0154, NGGR1392, NGGT2088, NGHQ2161 |
|---|
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-0790-2024%22
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