Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The brand name of the device is AlgiNot Recalled by Kerr Corporation Due to The firm recalled the product because it may...
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 Kerr Corporation directly.
Affected Products
The brand name of the device is AlgiNot, a dental impression material. Product Part Numbers AlgiNot Intra Kit 34683 AlgiNot Volume Refills 34682 Lot Number 1-1017 AlgiNot is a Class II Medical Device. The device listing number this product is 0136496 and the establishment registration number for Kerr Corporation is 1815757. Intended as an alternative to traditional alginate materials.
Quantity: 45 kits and 87 refills
Why Was This Recalled?
The firm recalled the product because it may cure harder than expected within the shelf life, which could result in a material that may be more difficult to remove. Use of this product on patients with loose teeth may result in possible tooth fracture or tooth extraction.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Kerr Corporation
Kerr Corporation has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report