Class II

Medical Device Recall: Bard¿ Nasogastric Sump Tube with ENFit, 12Fr., 48in Long, REF EN0042120

C.R. Bard Inc · December 20, 2023

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.

Distribution

US

Quantity Affected

6704 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0791-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

C.R. Bard Inc Medical Device Recall: Bard¿ Nasogastric Sump Tube with ENFit, 12Fr., 48in Long, REF EN0042120 | SafeCheck