C.R. Bard Inc: Medical Device Recall in 2024 - (Recall #: Z-0806-2024)

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¿ Suction Connector with ENFit, REF EN0066000

Product Classification:

Class II

Date Initiated: December 20, 2023

Date Posted: January 31, 2024

Recall Number: Z-0806-2024

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: 133610 units

Code Information:

UDI/DI 00801741128707, Lot/Serial Numbers: NGFS2792, NGFS4371, NGFV1647, NGFV1669, NGGN1988, NGGN2930, NGGN3517, NGGP0451, NGGP1098, NGGV0739, NGGV2722, NGGV5069, NGGW4456, NGGX3169, NGGZ0564, NGGZ1915, NGHP2225, NGHQ2201, NGHR0090, NGHS1005, NGHS1006, NGHS2421, NGHS3331, NGHU0845, NGHU1555, NGHV0467, NGHV2758, NGHW3025, NGHX1021, NGHX3269

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated