Jacksonville, FL, United States
Anjon Holdings recalls
1 recall recorded since 2018, most recently on 18 June 2020. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 18 June 2020
- Terminated
- 25 November 2020
- Reason
- High rate of galling of one threaded component.
- Distribution
- Worldwide distribution - US Nationwide distribution including in the state of MI and the country of Japan for training purposes.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2778-2020
- 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 fo
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.