Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) 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 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.
Quantity: 70 units
Why Was This Recalled?
The LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Neocis Inc.
Neocis Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report