C.R. Bard Inc: Medical Device Recall in 2024 - (Recall #: Z-0797-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit", 12Fr., 48in Long, REF EN0046120

Product Classification:

Class II

Date Initiated: December 20, 2023

Date Posted: January 31, 2024

Recall Number: Z-0797-2024

Event ID: 93679

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.

Status: Ongoing

Product Quantity: 26100 units

Code Information:

UDI/DI 00801741113239, Lot/Serial Numbers: NGDT1998, NGDZ3287, NGEU0889, NGEU2134, NGEV2411, NGEW2655, NGEY1506, NGEZ0664, NGFN4265, NGFU4024, NGFV3514, NGFW1857, NGFX0168, NGFX2645, NGGQ8458, NGGR2705, NGGX4777

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated