Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with… — Class II medical device recall Z-0796-2024
Ongoing recall by C.R. Bard Inc, reported 2024-01-31. BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Conn
| Recall number | Z-0796-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | C.R. Bard Inc, Covington, GA, United States |
| Recall initiated | 2023-12-20 |
| Classified | 2024-01-25 |
| Reported by FDA | 2024-01-31 |
| Quantity | 6,600 units |
| UPC / GTIN / UDI-DI | 00801741113222 |
| Serial numbers | NGDX0768, NGDZ3314, NGER3568, NGFT5023, NGFV3443, NGFW1904, NGFX0156, NGFX5525, NGGQ8459, NGGW4504 |
| Model numbers | EN0046100 |
Product
Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 10Fr., 36in Long, REF EN0046100
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0796-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.