Spine Wave recalls

Spine Wave appears in 2 official U.S. recall notices indexed by RecallRadar, most recently on 2015-07-08.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Spine Wave Access Kit, Catalog Number 10-1530 Package contents: RLSP494-Rhythmlink Monopolar Stimulating Probe and 10-1525 Disposable Dilat…
  FDA Device · Class II · 2015-07-08 · Spine Wave
• StaXx¿ IB Convex Expandable Implant (25 x 12 x 9 mm), Intervertebral Fusion Device, Lumbar
  FDA Device · Class II · 2013-09-18 · Spine Wave