C.R. Bard Inc: Medical Device Recall in 2024 - (Recall #: Z-0795-2024)

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¿ PreVent¿ Anti-Reflux Filter with ENFit, REF EN0046000

Product Classification:

Class II

Date Initiated: December 20, 2023

Date Posted: January 31, 2024

Recall Number: Z-0795-2024

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: 39430 units

Code Information:

UDI/DI 00801741113765, Lot/Serial Numbers: NGEV2409, NGEY1492, NGEY2717, NGEZ0908, NGEZ1657, NGEZ2692, NGFQ4105, NGFR1077, NGFR2312, NGFR3259, NGFS1627, NGFS4431, NGFT5468, NGFU1877, NGFU3837, NGFV1652, NGFV3513, NGFW1856, NGFX0167, NGFX2672, NGFX5611, NGGP3169, NGGT3611

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated