Zimmer Spine, Inc.
Minneapolis, MN
This page shows every FDA and USDA recall linked to Zimmer Spine, Inc.. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
6
Total Recalls
2004
First Recall
2016
Most Recent
Instinct Java System (IFU reference: 046WAN0000T) .
Stabilizes one or more vertebral segments from the thorac...
Feb 12, 2016
· Device
Terminated
Universal Clamp System (IFU reference: SNA027-N-90001).
Provides the stability required for solid bone fusion...
Feb 12, 2016
· Device
Terminated
Virage OCT Spinal Fixation System. Intended to promote fusion of the Occipital-Cervical-Thoracic spine (Occi...
Feb 3, 2016
· Device
Terminated
Zimmer Spine ST360 Distal Thread Reduction Guide Pins, Part number: 07.00684.00. Non-Sterile. Zimmer Spine,...
Nov 16, 2006
· Device
Terminated
Trinica Bone Tap Instrument, Catalog Number 07.00168.001, sold separately and as part of Zimmer Spine Trinica...
Feb 24, 2005
· Device
Terminated
ATO Drill Guide Kit (All Through One Drill Guides Set), model number 07.00860.001, product is packaged in tray...
Oct 23, 2004
· Device
Terminated