Burnsville, MN, United States
Advanced Research Medical, LLC recalls
1 recall recorded since 2018, most recently on 14 March 2023. 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
Completed Class II Medical devices
- Recall started
- 14 March 2023
- Reason
- Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Assembly during surgery.
- Distribution
- US Nationwide distribution in the state of Minnesota.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1698-2024
- ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop Blade, Part # 01-06-4; treatment of degenerative disc disease
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.