Drug recall
Bard¿ Lopez Valve¿ with ENFit, REF EN0056000
FDA recall event 93679 · Class II · C.R. Bard Inc
Key facts
| Event ID | 93679 |
|---|---|
| Recall numbers | Z-0790-2024, Z-0791-2024, Z-0792-2024, Z-0793-2024, Z-0794-2024, Z-0795-2024, Z-0796-2024, Z-0797-2024, Z-0798-2024, Z-0799-2024, Z-0800-2024, Z-0801-2024 and 5 more |
| Recalling firm | C.R. Bard Inc |
| Product type | Devices |
| Products | Bard¿ Lopez Valve¿ with ENFit, REF EN0056000, Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 12Fr., 48in Long, REF EN0056120, Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 18Fr., 48in Long, REF EN0056180, Bard¿ Nasogastric Sump Tube and PreVent¿ Filter and Lopez Valve¿ with ENFit, 14Fr., 48in Long, REF EN0056140, Bard¿ Nasogastric Sump Tube and PreVent¿ Filter and Lopez Valve¿ with ENFit, 16Fr., 48in Long , REF EN0056160 and 12 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Dec 20, 2023 |
| Report date | Jan 31, 2024 |
| City | Covington |
| State | GA |
| Country | United States |
| FEI number | 1018233 |
At a glance
- 10–99 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: