Reported Jan 20, 2016 · Terminated
Cavity 8 Gauge Spine Wand indicated for resection, ablation, and coagulation of soft tissues and hemostasis of blood…
ArthroCare Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: ArthroCare Corporation · 7000 W William Cannon Dr · Austin, TX · 78735-8509
Is this the product you have?
- Cavity 8 Gauge Spine Wand indicated for resection, ablation, and coagulation of soft tissues and hemostasis of blood vessels in spinal procedures.
- Lot codes and dates
- Lot Numbers
102431310244821027160103430610418791059328
- Lot Numbers
- Amount recalled
- 262 units
Where it was sold
Why it was recalled
There is cracking in the tray when the device is snapped into place. The crack is through the full thickness of the tray, compromising the sterile barrier.
This product could cause temporary or reversible health problems — stop using it.
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