Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Augmedics Perc Pin Adaptor Recalled by Augmedics Ltd. Due to The perc pin adaptor AMCH07200 tightening knob was...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Augmedics Ltd. directly.
Affected Products
Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation system that is designed to assist surgeons in placing pedicle screws accurately, during open or percutaneous computer-assisted spinal surgery.
Quantity: 85 units
Why Was This Recalled?
The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient to the user and the tightening markings found to be improperly placed.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Augmedics Ltd.
Augmedics Ltd. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report