FDA Recall Terminated

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.

Recall: Z-2778-2020 · Initiated June 18, 2020

Recall

Recall Number
Z-2778-2020
Event Number
85958
Firm
Anjon Holdings
FEI Number
3003346235
Product Code
JEC
Status
Terminated
Root Cause
Device Design
Initiated
June 18, 2020
Terminated
November 25, 2020
Address
4801 Dawin Rd, Jacksonville, FL, 32207-9512

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.

Reason

High rate of galling of one threaded component.

Action

The one unit released into the United States has already been returned, unused, to Anjon. No uncorrected product remains in distribution or in use in the USA. No units subject to the failure mode have been released into distribution within Japan. All units shipped to Japan are being either returned to Anjon for reprocessing to remove the failure mode; or are to corrected by the addition of the instruction to use sterile surgical lubricant on the thread of the Slider. JMDM is the license holder for the product within Japan and will not release the product until resolution to its satisfaction of the issue.

Distribution

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

Quantity

249 devices