Bard¿ Lopez Valve¿ with ENFit — Class II medical device recall Z-0801-2024
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-0801-2024 |
|---|---|
| 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 | 187,550 units |
| UPC / GTIN / UDI-DI | 00801741113901 |
| Serial numbers | NGFU2486, NGFU3807, NGFW1859, NGFX0062, NGFX5625, NGFY0610, NGFZ1664, NGGR0346, NGGR2172, NGGS0703, NGGS2557, NGGS3418, NGGYY001, NGHN0893, NGHQ3357, NGHQ3358, NGHQ3359, NGHQ3383, NGHQ3384, NGHR0028, NGHR0029, NGHR0030, NGHR0031, NGHR0032, NGHR0072 and 14 more |
| Model numbers | EN0056000 |
Product
Bard¿ Lopez Valve¿ with ENFit, REF EN0056000
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-0801-2024. 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.