C.R. Bard Inc: Medical Device Recall in 2024 - (Recall #: Z-0800-2024)

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, 18Fr., 48in Long, REF EN0046180

Product Classification:

Class II

Date Initiated: December 20, 2023

Date Posted: January 31, 2024

Recall Number: Z-0800-2024

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: 57159 units

Code Information:

UDI/DI 00801741113260, Lot/Serial Numbers: NGDT2000, NGDX0518, NGEW1822, NGEW3855, NGEX0043, NGEX1998, NGEZ2693, NGFP0406, NGFP3519, NGFR0244, NGFT0418, NGFT3481, NGFU3821, NGFV0785, NGFV1654, NGFV3445, NGFW1906, NGFX0169, NGFX2674, NGFX5527, NGGP3171

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated