Peter Lazic Gmbh: Medical Device Recall in 2024 - (Recall #: Z-1279-2024)

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:

D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.

Product Classification:

Class II

Date Initiated: October 6, 2023

Date Posted: March 20, 2024

Recall Number: Z-1279-2024

Event ID: 93938

Reason for Recall:

Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.

Status: Ongoing

Product Quantity: 10 units

Code Information:

Model number: 35.412; UDI/DI: 04250603739616; All Lot numbers.

Distribution Pattern:

US Nationwide distribution in the state of ME.

Voluntary or Mandated:

Voluntary: Firm initiated