Burke, VA, United States
Neuropro Spinal Jaxx recalls
1 recall recorded since 2018, most recently on 18 January 2018. 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 January 2018
- Terminated
- 13 July 2018
- Reason
- The implant size is incorrectly etched on the implant. The size listed on the box is correct.
- Distribution
- The devices were distributed in California.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1350-2018
- Spinal Jaxx Interbody Fusion Device, Model: 100001-511, Size: 9 H x 10 W x 25 L Product Usage: The Spinal Jaxx interbody fusion device is indicated for spinal fusion for patients with degenerative disc disease (DDD)
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.