New Wave Endo-Surgical, Corp.: Medical Device Recall in 2023 - (Recall #: Z-1570-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and needle guide for the abdominal wall

Product Classification:

Class II

Date Initiated: July 8, 2020

Date Posted: May 17, 2023

Recall Number: Z-1570-2023

Event ID: 92005

Reason for Recall:

The plastic housing on the device may fracture

Status: Terminated

Product Quantity: 295 units

Code Information:

UDI/DI: 00850009417022, Lot code C2020

Distribution Pattern:

US Nationwide distribution in the states of FL, MA, and GA.

Voluntary or Mandated:

Voluntary: Firm initiated