Anjon Holdings: Medical Device Recall in 2020 - (Recall #: Z-2778-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Anjon Bremer Molded Crown. bone fixation fastener for spinal use. REF number 100048 - Product Usage: Smooth or threaded metallic bone fixation fastener. Provides cervical spine immobilization and therapeutic traction for treatment of patients with cervical trauma or other neck conditions.

Product Classification:

Class II

Date Initiated: June 18, 2020

Date Posted: August 19, 2020

Recall Number: Z-2778-2020

Event ID: 85958

Reason for Recall:

High rate of galling of one threaded component.

Status: Terminated

Product Quantity: 249 devices

Code Information:

REF number 100048 Lot # 170240, US customer Lot # 170162, 170163, 70164,170165, 170229, 170240, 170247, 170260 and SM 42048. International customers.

Distribution Pattern:

Worldwide distribution - US Nationwide distribution including in the state of MI and the country of Japan for training purposes.

Voluntary or Mandated:

Voluntary: Firm initiated