Aesculap Implant Systems LLC: Medical Device Recall in 2022 - (Recall #: Z-1405-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.

Product Classification:

Class II

Date Initiated: June 30, 2021

Date Posted: July 27, 2022

Recall Number: Z-1405-2022

Event ID: 90537

Reason for Recall:

Customized coronal rod benders may deform the implant when used with the spinal system devices.

Status: Terminated

Product Quantity: 2 pieces

Code Information:

LOT: 2930902A

Distribution Pattern:

United States: CO

Voluntary or Mandated:

Voluntary: Firm initiated