C.R. Bard Inc: Medical Device Recall in 2024 - (Recall #: Z-0798-2024)

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, 14Fr., 48in Long, REF EN0046140

Product Classification:

Class II

Date Initiated: December 20, 2023

Date Posted: January 31, 2024

Recall Number: Z-0798-2024

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: 36440 units

Code Information:

UDI/DI 00801741113246, Lot/Serial Numbers: NGDT1999, NGDU4285, NGDX0617, NGES3429, NGET1383, NGEU2115, NGEV4551, NGEX1978, NGEY0623, NGEY2687, NGFN0745, NGFN4316, NGFQ4111, NGFV3444, NGFW1905, NGFX2673, NGFX5526, NGGT4255, NGGU4246, NGGX5757

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated