Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left) Recalled by Neocis, Inc. Due to Mislabeling
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 Neocis, Inc. directly.
Affected Products
DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left); accessories to the parent system, the Neocis Guidance System (NGS)
Quantity: 100 units
Why Was This Recalled?
The LRUL and LLUR posterior chairside splints and the LLUR anterior chairside splints may be mislabeled.
Where Was This Sold?
This product was distributed to 7 states: AZ, CT, FL, MA, NY, OH, PA
About Neocis, Inc.
Neocis, Inc. 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